A novel locus for autosomal dominant non‐syndromic deafness, DFNA53, maps to chromosome 14q11.2‐q12

BACKGROUND: Non‐syndromic hearing loss is among the most genetically heterogeneous traits known in humans. To date, at least 50 loci for autosomal dominant non‐syndromic sensorineural hearing loss (ADNSSHL) have been identified by linkage analysis. OBJECTIVE: To report the mapping of a novel autosom...

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Detalhes bibliográficos
Main Authors: Yan, D, Ke, X, Blanton, S H, Ouyang, X M, Pandya, A, Du, L L, Nance, W E, Liu, X Z
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2006
Assuntos:
Letter to JMG
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2564639/
https://ncbi.nlm.nih.gov/pubmed/15958501
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.034710
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