A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval.
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Evidence for changes in beta- and gamma-actin proportions during inner ear hair cell lifeA mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).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.Audiometric and vestibular features in a second Dutch DFNA20/26 family with a novel mutation in ACTG1.
P2860
A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval.
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2003 nî lūn-bûn
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A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval.
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A second kindred linked to DFNA20
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A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval.
@en
A second kindred linked to DFNA20
@nl
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A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval.
@en
A second kindred linked to DFNA20
@nl
P1433
P1476
A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval
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P2093
P356
10.1034/J.1399-0004.2003.630106.X
P577
2003-01-01T00:00:00Z