Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
about
Viral infection and human disease--insights from minimotifsMotif mediated protein-protein interactions as drug targetsEarly detection of hearing lossDeafness mutation mining using regular expression based pattern matching.Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation.Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).A DNA variant within the MYO7A promoter regulates YY1 transcription factor binding and gene expression serving as a potential dominant DFNA11 auditory genetic modifierVestibular function in families with inherited autosomal dominant hearing loss.Myosin light chains: Teaching old dogs new tricksIn search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier.Genetics and pathological mechanisms of Usher syndrome.Auditory and vestibular hair cell stereocilia: relationship between functionality and inner ear disease.Mild and variable audiometric and vestibular features in a third DFNA15 family with a novel mutation in POU4F3.Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China.Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
P2860
Q24647289-84BEC4FF-891A-4A71-A469-DAF5CBB8F9B8Q28079554-4D031206-05A6-40A3-93A4-4BFCC5652B14Q30472998-6F5CF090-7807-4AE5-BAB5-8B801993E120Q33303929-92B846E1-6DDB-462E-95E3-64D72B0F2D58Q33936748-C5929E3A-2691-43A1-8582-A43745DCA281Q34576163-81861261-3FB0-42E8-8F8A-3722B3690AFAQ34869496-4252BC38-AEBF-490F-AB8C-68B6F6CB4CF5Q36955586-14626943-8368-49C2-8465-27CAAC0FC860Q37021389-C2FBCB2E-CCFF-44EC-82AE-20CC352FDE02Q37110827-3CA5658C-AEA8-42FB-8792-58A4AC7B5DF1Q37727784-F80563A4-1844-4D8C-8226-406F084F3D3AQ37903075-AFC8CB19-49F3-48E1-9D8C-7500030DAC15Q44406379-5ED174AB-32CE-42CF-BE88-F49454D14359Q50435636-940A8405-0404-4113-BABE-CF66B4B7438DQ50453784-CFC647C8-C47F-4970-BD4F-0D4ABEFAB368
P2860
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
description
2004 nî lūn-bûn
@nan
2004 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@ast
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@en
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@en-gb
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@nl
type
label
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@ast
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@en
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@en-gb
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@nl
prefLabel
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@ast
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@en
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@en-gb
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@nl
P2093
P356
P1433
P1476
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)
@en
P2093
Andreas Gal
Christian Kothe
Gerrit Mohrmann
Götz Schade
Hanno Bolz
Markus Hess
Steffen-Sebastian Bolz
P356
10.1002/HUMU.9272
P407
P577
2004-09-01T00:00:00Z