טוען...
DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22–q21.12
This article describes the identification of a novel locus (DFNB39) responsible for an autosomal recessive form of hearing loss segregating in a Pakistani consanguineous family. The hearing impaired members of this family present with profound prelingual sensorineural hearing impairment and use sign...
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| Main Authors: | , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2003
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2909101/ https://ncbi.nlm.nih.gov/pubmed/14512973 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5201041 |
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