Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p
about
A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemiaMutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairmentCellular and molecular mechanisms of autosomal dominant form of progressive hearing loss, DFNA2.Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment.Non-syndromic autosomal-dominant deafness.The genetic bases for non-syndromic hearing loss among ChineseKCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing lossDigenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31Inherited hearing loss: molecular genetics and diagnostic testing.Longitudinal and cross-sectional phenotype analysis in a new, large Dutch DFNA2/KCNQ4 family.
P2860
Q24309111-EE1CCC38-7A45-4424-93E7-0AAA3D259FE0Q28290745-2366BC73-DEF7-46A6-8A5E-4738DB931EE9Q30497891-FD68CC2A-8EDC-4B36-9878-4762F2A96D66Q33783963-7E4CF948-B1C6-4ECE-B4D3-487188E8F19BQ33881296-131F40F8-AE18-4E58-9EF9-B9DB18DCE988Q33912298-93EFAD8B-26CC-4C3F-B96D-B61CB070A2F0Q33965187-092FA82E-015B-4735-BB89-D5ADDD42CAFCQ34138254-3C10108F-A111-442C-A2C7-895A5C802014Q34747004-258700F1-F83A-4EB3-AC97-B82137B89837Q35879586-926FF04B-4C19-4153-A5BC-E818A48B5659Q37271361-1ED75432-7555-436D-98FB-EC3E25195C11Q37332766-EB0DAD65-C0F7-434C-A230-DC71C0A7DD48Q38089731-EBD54F20-D36D-41CB-8EE6-B440EA337871Q50488412-46F1B5FF-C69D-4902-AF4E-88D474A229C9
P2860
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p
description
1997 nî lūn-bûn
@nan
1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@ast
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@en
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@nl
type
label
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@ast
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@en
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@nl
prefLabel
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@ast
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@en
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@nl
P2093
P356
P1433
P1476
Linkage analysis of progressiv ...... .25-Mb region on chromosome 1p
@en
P2093
Cremers CW
Djelantik B
Schatteman I
P356
10.1006/GENO.1997.4624
P407
P577
1997-04-01T00:00:00Z