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MYO7A gene

Known as: NSRD2, MYOSIN, UNCONVENTIONAL, FAMILY VII, MEMBER A, MYU7A 
National Institutes of Health

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Related topics

3 relations
DEAFNESS, AUTOSOMAL RECESSIVE 2MYO3A genemyosin VIIa

Papers overview

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2020
2020
The p.R206C Mutation in MYO7A Leads to Autosomal Dominant Nonsyndromic Hearing Loss
Background: Dominant mutations in MYO7A may lead to nonsyndromic deafness DFNA11. A p.R206C variant in MYO7A has previously been… 
2018
2018
A Novel Homozygous MYO7A Mutation: Case Report
MYO7A is an unconventional myosin that is essential for ordinary hearing and vision; mutations in the MYO7A gene result in Usher… 
2018
2018
Leber Congenital Amaurosis in Asia
Leber congenital amaurosis (LCA) is a heterogeneous infantile retinal dystrophy presenting with severe visual loss, nystagmus… 
2015
2015
A novel MYO7A compound heterozygous mutation in an USH1 portuguese patiant : a translational multidisciplinary study
2014
2014
Detecting novel genetic mutations in Chinese Usher syndrome families using next-generation sequencing technology
Usher syndrome (USH) is the most common cause of combined blindness and deafness inherited in an autosomal recessive mode… 
2008
2008
Анализ генов 12SrRNA, tRNASer(UCN), MYO7A и USH2A у пациентов с наследственными формами нарушения зрения и слуха
2003
2003
The molecular genetics of Usher syndrome
Association of sensorineural deafness and progressive retinitis pigmentosa with and without a vestibular abnormality is the…