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Apcdd1 is a novel Wnt inhibitor Mutated in Hereditary Hypotrichosis Simplex
Hereditary hypotrichosis simplex (HHS) is a rare autosomal dominant form of hair loss characterized by hair follicle (HF) miniaturization1, 2. Using genetic linkage analysis, we mapped a novel locus for HHS to chromosome 18p11.22, and identified a mutation (L9R) in the APCDD1 gene in three families....
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| Autori principali: | , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3046868/ https://ncbi.nlm.nih.gov/pubmed/20393562 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature08875 |
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