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- W1982190261 abstract "Monilethrix, an autosomal dominant human hair disorder, is caused by mutations in three type II hair cortex keratins. Rare cases of the disease with non-vertical transmission have now been found to overlap with localized autosomal recessive hypotrichosis. The underlying gene, desmoglein 4 (DSG4), belongs to the desmosomal cadherin superfamily and is also expressed in the cortex of the hair follicle." @default.
- W1982190261 created "2016-06-24" @default.
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- W1982190261 date "2006-06-01" @default.
- W1982190261 modified "2023-10-13" @default.
- W1982190261 title "More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players" @default.
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- W1982190261 doi "https://doi.org/10.1038/sj.jid.5700266" @default.
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