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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主要な著者: Shimomura, Yutaka, Agalliu, Dritan, Vonica, Alin, Luria, Victor, Wajid, Muhammad, Baumer, Alessandra, Belli, Serena, Petukhova, Lynn, Schinzel, Albert, Brivanlou, Ali H., Barres, Ben A., Christiano, Angela M.
フォーマット: Artigo
言語:Inglês
出版事項: 2010
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Article
オンライン･アクセス: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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