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Publications by Maryam Shirzad
Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of C.299-300delAT Mutation in Kurdish Population of Iran
Journal of audiology and otology
Otorhinolaryngology
Sensory Systems
Speech
Hearing
Related publications
Mutation of COL11A2 Causes Autosomal Recessive Non-Syndromic Hearing Loss at the DFNB53 Locus
Journal of Medical Genetics
Genetics
GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss
Revista Romana de Medicina de Laborator
Identification of a Novel Homozygous Mutation, TMPRSS3: C.535G>A, in a Tibetan Family With Autosomal Recessive Non-Syndromic Hearing Loss
PLoS ONE
Multidisciplinary
Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53
Molecular Genetics and Genomics
Medicine
Genetics
Molecular Biology
Genotype-Phenotype Correlation Analysis of MYO15A Variants in Autosomal Recessive Non-Syndromic Hearing Loss
BMC Medical Genetics
Genetics
Novel Recessive PDZD7 Biallelic Mutations in Two Chinese Families With Non-Syndromic Hearing Loss
American Journal of Medical Genetics, Part A
Genetics
Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss
Zahedan Journal of Research in Medical Sciences
GJB2 ‐related Hearing Loss in Central Iran: Review of the Spectrum and Frequency of Gene Mutations
Annals of Human Genetics
Genetics
Carrier Frequency of the GJB2 Mutations That Cause Hereditary Hearing Loss in the Japanese Population
Journal of Human Genetics
Genetics
