HOME PRODUCTS COMPANY CONTACT FAQ

Research Dictionary Pharma

Sign Up FREE or Login

Autosomal Dominant 48 Deafness

mutation in MYO1A

Also Known As:

Deafness, Autosomal Dominant 48; DFNA48

Networked: 3 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1.	Nonsyndromic Deafness
2.	Hearing Loss (Hearing Impairment)
3.	Deafness (Deaf Mutism)
4.	Autosomal Recessive 30 Deafness
5.	Autosomal Recessive 37 Deafness

Experts

1.	Baig, Shahid M: 1 article (05/2014)
2.	Bergmann, Carsten: 1 article (05/2014)
3.	Beyer, Anke: 1 article (05/2014)
4.	Bolz, Hanno J: 1 article (05/2014)
5.	Decker, Christian: 1 article (05/2014)
6.	Decker, Eva: 1 article (05/2014)
7.	Di Donato, Nataliya: 1 article (05/2014)
8.	Eisenberger, Tobias: 1 article (05/2014)
9.	Mürbe, Dirk: 1 article (05/2014)
10.	Neuhaus, Christine: 1 article (05/2014)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Autosomal Dominant 48 Deafness:

1.	Myosin Type I (Myosin IA)IBA 06/01/2003 - "MYO1A, which is located within the DFNA48 locus, is the first myosin I family member found to be involved in causing deafness and may be a major contributor to autosomal dominant-hearing loss."
2.	Nonsense Codon (Nonsense Mutation)IBA 05/01/2014 - "MYO1A is considered the gene underlying autosomal dominant nonsyndromic hearing loss DFNA48, based on six missense variants, one small in-frame insertion, and one nonsense mutation. "
3.	Myosins (Myosin)IBA 04/15/2008 - "Seven different unconventional myosin genes are involved in ten different types of syndromic and nonsyndromic hearing loss with different patterns of inheritance: MYO7A in DFNA11/DFNB2/USH1B, MYH9 in DFNA17, MYH14 in DFNA4, MYO6 in DFNA22/DFNB37, MYO3A in DFNB30, MYO1A in DFNA48, and MYO15A in DFNB3. "