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A locus for hereditary hypotrichosis localized to human chromosome 18q21.1
Hereditary hypotrichosis is a rare autosomal recessive condition characterized clinically by alopecia. Three consanguineous kindreds with multiple affected individuals were ascertained from different regions of Pakistan. A novel hypotrichosis locus was mapped to a 5.5 cM region on chromosome 18q21.1...
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| Publicado no: | Eur J Hum Genet |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6157268/ https://ncbi.nlm.nih.gov/pubmed/12891384 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5201005 |
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