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Molecular Biology Reports, ISSN 0301-4851, 8/2019, Volume 46, Issue 4, pp. 4105 - 4111
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 4/2018, Volume 55, Issue 4, pp. 3477 - 3489
Journal Article
Clinical and Experimental Optometry, ISSN 0816-4622, 03/2018, Volume 101, Issue 2, pp. 255 - 259
Background: Norrie disease (ND) is a rare, X-linked recessive disorder with the main characteristic of early childhood blindness. The aim of the present study... 
mutation | Iranian | pseudoglioma | Norrie disease | blindness | EXUDATIVE VITREORETINOPATHY | FZD4 | OPHTHALMOLOGY | CANDIDATE GENE | Genetic research | Genetic aspects | Codon | Genes | Blindness | NDP gene | Frameshift mutation | Insertion | Stop codon | Children | Mutation | Males | Hereditary diseases | Index Medicus
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 4/2017, Volume 54, Issue 3, pp. 2234 - 2240
Journal Article
Genetic Testing and Molecular Biomarkers, ISSN 1945-0265, 08/2017, Volume 21, Issue 8, pp. 485 - 490
Journal Article
Clinical Laboratory, ISSN 1433-6510, 2019, Volume 65, Issue 4, pp. 517 - 525
Background: Schizophrenia (SCZ) is a serious mental disorder that interferes with a person's cognitive processes and leads to social disability. A wide range... 
QPCR | Schizophrenia | Gene expression | RAB8B | TRANSPORT | INTERACTING PARTNER | TRAFFICKING | qPCR | schizophrenia | AUTOPHAGY | MEDICAL LABORATORY TECHNOLOGY | GTPASE | gene expression
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 05/2019, Volume 40, Issue 3, pp. 259 - 266
Purpose: Cone-rod dystrophy (CRD) is an inherited retinal dystrophy that is transmitted via different modes of inheritance. Mutations in more than 30 genes... 
incomplete penetrance | autosomal recessive inheritance pattern | Cone-rod dystrophy | CRX gene | GENETICS & HEREDITY | OPHTHALMOLOGY | MUTATIONS | HOMEOBOX GENE | ABCA4 GENE
Journal Article
Ophthalmic genetics, 06/2019, p. 1
: Cone-rod dystrophy (CRD) is an inherited retinal dystrophy that is transmitted via different modes of inheritance. Mutations in more than 30 genes have been... 
Journal Article
International Journal of Molecular and Cellular Medicine, ISSN 2251-9637, 2017, Volume 6, Issue 4, pp. 204 - 211
In the current study, we conducted a mutation screening of tumor-associated calcium signal transducer 2 ( ) gene in six consanguineous Iranian families with... 
GDLD; TACSTD | Iranian | Corneal dystrophy | Gelatinous drop-like | Studies | Cornea | Algorithms | Microscopy | Genes | Colorectal cancer | Mutation | Patients | Bioinformatics | corneal dystrophy | Original
Journal Article
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