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Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation
While there have been significant advances in understanding the genetic etiology of human hair loss over the previous decade, there remain a number of hereditary disorders for which a causative gene has yet to be identified. We studied a large, consanguineous Brazilian family that presented with spa...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3341170/ https://ncbi.nlm.nih.gov/pubmed/18692127 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ygeno.2008.06.009 |
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