Dominant modifier DFNM1 suppresses recessive deafness DFNB26.

Riazuddin, S; Castelein, C M; Ahmed, Z M; Lalwani, A K; Mastroianni, M A; Naz, S; Smith, T N; Liburd, N A; Friedman, T B; Griffith, A J; Riazuddin, S; Wilcox, E R

Riazuddin, S; Castelein, C M; Ahmed, Z M; Lalwani, A K; Mastroianni, M A; Naz, S; Smith, T N; Liburd, N A; Friedman, T B; Griffith, A J; Riazuddin, S; Wilcox, E R.

Affiliation

Riazuddin S; Laboratory of Molecular Genetics, NIDCD/NIH, Rockville, Maryland, USA.

Nat Genet ; 26(4): 431-4, 2000 Dec.

Article in En | MEDLINE | ID: mdl-11101839

Subject(s)

Deafness/genetics; Chromosome Mapping; Chromosomes, Human, Pair 1/genetics; Chromosomes, Human, Pair 4/genetics; Connexin 26; Connexins; Consanguinity; Female; Genes, Dominant; Genes, Recessive; Haplotypes; Humans; Lod Score; Male; Microsatellite Repeats; Pedigree; Suppression, Genetic

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Collection: 01-internacional Database: MEDLINE Main subject: Deafness Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Nat Genet Year: 2000 Document type: Article

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