Amanote Research
Register
Sign In
Non-Syndromic Recessive Auditory Neuropathy Is the Result of Mutations in the Otoferlin (OTOF) Gene
Journal of Medical Genetics
- United Kingdom
doi 10.1136/jmg.40.1.45
Full Text
Open PDF
Abstract
Available in
full text
Categories
Genetics
Date
January 1, 2003
Authors
R Varga
Publisher
BMJ
Related search
Novel OTOF Mutations in Brazilian Patients With Auditory Neuropathy
Journal of Human Genetics
Genetics
Q829X, a Novel Mutation in the Gene Encoding Otoferlin (OTOF), Is Frequently Found in Spanish Patients With Prelingual Non-Syndromic Hearing Loss
Journal of Medical Genetics
Genetics
Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53
Molecular Genetics and Genomics
Medicine
Genetics
Molecular Biology
Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Novel Recessive PDZD7 Biallelic Mutations in Two Chinese Families With Non-Syndromic Hearing Loss
American Journal of Medical Genetics, Part A
Genetics
Periaxin Mutations Cause Recessive Dejerine-Sottas Neuropathy
American Journal of Human Genetics
Genetics
Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome
American Journal of Human Genetics
Genetics
Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Mutation of COL11A2 Causes Autosomal Recessive Non-Syndromic Hearing Loss at the DFNB53 Locus
Journal of Medical Genetics
Genetics