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Connexin 26 and autosomal recessive non-syndromic hearing loss, 07/2003
Prelingual deafness occurs with a frequency of 1 in 1000 live births and is divided into syndromic and non-syndromic forms contributing 40 and 60%... 
hg03010 Non-syndromic, Hearing loss, Autosomal recessive, Connexin 26, DFNB1, mutation detection, Gap junction proteins, GJB2 | Genetics
Journal
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, pp. e0176516 - e0176516
The MYO7A gene encodes a protein belonging to the unconventional myosin super family. Mutations within MYO7A can lead to either non syndromic hearing loss or... 
PROTEIN STABILITY | DFNB2 | USHER-SYNDROME | SYNDROME TYPE 1B | SERVER | MULTIDISCIPLINARY SCIENCES | PHENOTYPE | DEAFNESS | SPECTRUM | MYOSIN-VIIA GENE | MISSENSE MUTATIONS | Humans | Models, Molecular | Male | Myosins - chemistry | Myosins - genetics | Exome | Morocco | Usher Syndromes - genetics | Pedigree | Adult | Female | Heterozygote | Mutation | Care and treatment | Gene mutations | Analysis | Genetic aspects | Research | Muscle proteins | Risk factors | Hearing loss | Impact prediction | Gait | Lung | Retina | Hearing protection | Fragmentation | Proteins | Alterations | Coding | Cell adhesion | Genetics | Libraries | Diagnosis | Cell body | Deoxyribonucleic acid--DNA | Hair | Evaluation | Deafness | Pathogens | Human motion | Amino acid sequence | Nucleic acids | Adaptors | Cadherin | Hereditary diseases | Pathogenicity | Hearing | Software packages | Plates (structural members) | Quality control | Cell migration | Methods | Kidney transplantation | Cargo | Audiometry | Structural stability | Laboratories | Identification methods | Retinitis pigmentosa | Exons | Genes | Missense mutation | Adhesive strength | Filaments | Actin | Kidneys | Chloroform | Nucleotide sequence | Hearing impairment | Computer programs | Cadherin 23 | Reagents | Speech | Gene mapping | Cancer | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 09/2018, Volume 112, pp. 188 - 192
Oxidative stress plays a key role in the formation of age-related, noise-induced and drug-induced hearing loss. Thiols are organic compounds which can react... 
Oxidative stress | Thiol | Autosomal recessive non-syndromic hearing loss | Disulphide | Hearing loss | PROTECTION | PREVENTION | THIOL/DISULPHIDE HOMEOSTASIS | OTOTOXICITY | NOISE | MECHANISMS | OTORHINOLARYNGOLOGY | PEDIATRICS | DEAFNESS | MUTATIONS | COMMUNICATION | Medical research | Care and treatment | Thiols | Gene mutations | Analysis | Medicine, Experimental | Free radicals (Chemistry) | Index Medicus
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 08/2015, Volume 463, Issue 4, pp. 582 - 586
Mutation of has been reported to cause autosomal dominant non-syndromic hearing loss (DFNA2A) that usually presents as progressive hearing loss starting from... 
Frameshift mutation | KCNQ4 | Autosomal recessive | Hereditary hearing loss | C-terminus | BIOCHEMISTRY & MOLECULAR BIOLOGY | HELIX | JERVELL | BIOPHYSICS | CHANNEL | GENE | CDH23 | DOMINANT DEAFNESS | LINKAGE | Hearing Loss - genetics | Frameshift Mutation | Pedigree | Humans | Long QT Syndrome - genetics | Adult | Female | Male | Genes, Recessive | KCNQ Potassium Channels - genetics | Index Medicus
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 04/2018, Volume 107, pp. 121 - 126
Hereditary hearing loss (HL) is a noticeable concern in medicine all over the world. On average, 1 in 166 babies born are diagnosed with HL in Iran, which... 
GJB2 | Iran | Autosomal recessive non-syndromic hearing loss | c.35delG | CONNEXIN-26 GJB2 | PREVALENCE | IMPAIRMENT | NORTH | CX26 GENE-MUTATIONS | FAMILIES | OTORHINOLARYNGOLOGY | FREQUENCY | PEDIATRICS | DEAFNESS | FOUNDER | Index Medicus
Journal Article
Iranian Journal of Public Health, ISSN 2251-6085, 05/2016, Volume 45, Issue 5, pp. 680 - 687
Journal Article
Iranian Rehabilitation Journal, ISSN 1735-3602, 09/2015, Volume 13, Issue 3, pp. 64 - 68
Objectives: Hearing loss (HL) is the most common sensory disorder, and affects 1 in 1000 newborns. About 50% of HL is due to genetics and 70% of them are... 
Homozygosity mapping | Iran | Autosomal recessive non-syndromic hearing loss | Linkage analysis
Journal Article
مجله دانشگاه علوم پزشکی گرگان, ISSN 1562-4765, 05/2014, Volume 16, Issue 2, pp. 82 - 88
Background and Objective: SLC26A4 gene mutations after GJB2 mutations are the second currently identifiable genetic cause of autosomal recessive non syndromic... 
Short Tandem Repeat | Ethnicity | SLC26A4 gene | Iran | D7S2456 marker | Autosomal recessive non syndromic hearing loss
Journal Article
Gene, ISSN 0378-1119, 08/2019, Volume 709, pp. 65 - 74
Journal Article
Majallah-i dānishgāh-i ̒ulūm-i pizishkī-i Arāk, ISSN 1735-5338, 06/2017, Volume 20, Issue 3, pp. 31 - 38
Abstract Background: Hearing loss (HL) is the most common congenital defect in humans. One or two in thousand newborn babies have prelingual hearing loss.... 
Genetic linkage | DFNB21 locus | Autosomal recessive non-syndromic hearing loss
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 05/2002, Volume 19, Issue 5, pp. 572 - 572
Hereditary hearing loss (HHL) is an extremely common disorder. About 70% of HHL is non‐syndromic, with autosomal recessive forms accounting for ∼85% of the... 
Connexin 26 | GJB2, Iranian | Cx26 | autosomal recessive non‐syndromic deafness, ARNSD | HHL | hereditary hearing loss | Hearing Disorders - genetics | Genes, Recessive - genetics | Humans | Connexins - genetics | Iran - epidemiology | Mutation - genetics | Genetic Testing - methods | Genetic Carrier Screening - methods | Syndrome | Index Medicus
Journal Article