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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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Detaylı Bibliyografya
Asıl Yazarlar: Yan, D, Ke, X, Blanton, S H, Ouyang, X M, Pandya, A, Du, L L, Nance, W E, Liu, X Z
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Group 2006
Konular:
Online Erişim: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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