A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment

Nanna Dahl Rendtorff,Mei Zhu,Toril Fagerheim,Torben L. Antal,Mary Pat Jones,Tanya M. Teslovich,Elizabeth M. Gillanders,M. Michael Barmada,Erik Teig,Jeffrey M. Trent,Karen H. Friderici,Dietrich A. Stephan,Lisbeth Tranebjærg

A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment

2006

Nanna Dahl Rendtorff
Mei Zhu
Toril Fagerheim
Torben L. Antal
Mary Pat Jones
Tanya M. Teslovich
Elizabeth M. Gillanders
M. Michael Barmada
Erik Teig
Jeffrey M. Trent
Karen H. Friderici
Dietrich A. Stephan
Lisbeth Tranebjærg

A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment

Keywords:

Hearing loss
Norwegian
Biology
Missense mutation
ACTG1
Genetics
Gene
Mutation
Dominance (genetics)
Bioinformatics
Locus (genetics)
Postlingual sensorineural hearing impairment

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