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Nature, ISSN 0028-0836, 10/2011, Volume 478, Issue 7367, pp. 57 - 63
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 01/2018, Volume 24, Issue 7, pp. 1 - 13
Journal Article
Journal Article
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 11/2019, Volume 126, pp. 109607 - 109607
Mutations in the gene encoding connexin 26 (Cx26) cause autosomal recessive and rarely dominant nonsyndromic sensorineural hearing loss as well as asyndromic... 
GJB2 | Nonsyndromic hearing loss | Palmoplantar keratoderma | De novo | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2011, Volume 108, Issue 30, pp. 12390 - 12395
Here we report a human intellectual disability disease locus on chromosome 14q31.3 corresponding to mutation of the ZC3H14 gene that encodes a conserved... 
Protein isoforms | Brain | Messenger RNA | Intellectual disability | RNA | Neurons | Drosophila | Genetic mutation | Human genetics | RNA binding proteins | RNA processing | Mental retardation | Zinc-finger | Polyadenylation | polyadenylation | mental retardation | NUCLEAR | LENGTH CONTROL | RECOGNITION | MULTIDISCIPLINARY SCIENCES | NAB2 | zinc-finger | EXPORT | POLY(A) POLYMERASE | RNA-Binding Proteins - genetics | Drosophila melanogaster - physiology | Humans | Molecular Sequence Data | Male | RNA, Messenger - metabolism | Drosophila melanogaster - genetics | Gene Knockdown Techniques | Intellectual Disability - genetics | Central Nervous System - physiology | Young Adult | Drosophila Proteins - physiology | Iran | Conserved Sequence | Adult | Female | Models, Animal | Nuclear Proteins - genetics | Amino Acid Sequence | RNA-Binding Proteins - physiology | RNA, Messenger - genetics | Chromosome Mapping | Genes, Recessive | Sequence Homology, Amino Acid | Flight, Animal - physiology | Hippocampus - metabolism | Animals | Pedigree | Adolescent | Zinc Fingers - genetics | Consanguinity | Nuclear Proteins - physiology | Drosophila Proteins - genetics | Mutation | Chromosomes, Human, Pair 14 - genetics | Cohort Studies | Evolution, Molecular | Adenosine | Neural circuitry | Gene mutations | Physiological aspects | Genetic aspects | Research | Gene expression | Binding proteins | Proteins | Nervous system | Insects | Index Medicus | Animal models | Flight | Central nervous system | Data processing | Locomotion | RNA-binding protein | chromosome 14 | Cell body | Hippocampus | Biological Sciences
Journal Article
2017 39th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC), ISSN 1557-170X, 07/2017, Volume 2017, pp. 2972 - 2975
Noninvasive brain computer interfaces (BCI), and more specifically Electroencephalography (EEG) based systems for intent detection need to compensate for the... 
Graphical models | Navigation | Xenon | Brain modeling | Probabilistic logic | Electroencephalography | Calibration | Index Medicus
Conference Proceeding
Journal of Human Genetics, ISSN 1434-5161, 2014, Volume 59, Issue 7, pp. 368 - 375
Bardet-Biedl syndrome (BBS) is a rare ciliopathy disorder that is clinically and genetically heterogeneous with 18 known genes. This study was performed to... 
DIAGNOSIS | COMPLEX | OBESITY | DISEASES | DATABASE | DNA | GENETICS & HEREDITY | IDENTIFICATION | FAMILY | Amino Acid Sequence | Humans | Molecular Sequence Data | Genotype | Male | Genetic Heterogeneity | Phenotype | Sequence Alignment | Iran | DNA Mutational Analysis | Base Sequence | Bardet-Biedl Syndrome - genetics | Female | Consanguinity | Mutation | Quantitative Trait Loci | Index Medicus
Journal Article
Journal Article