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DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3
Genetic analysis of an inbred Pakistani family PKDF280, segregating prelingual severe to profound sensorineural hearing loss, provided evidence for a DFNB locus on human chromosome 9q34.3. Co-segregation of the deafness trait with marker D9SH159 was determined by a two-point linkage analysis (LOD sc...
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| Autori principali: | , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2795002/ https://ncbi.nlm.nih.gov/pubmed/19603065 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2009.121 |
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