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Identification of two novel mutations in the PLCD1 gene in Chinese patients with hereditary leukonychia

Hereditary leukonychia (HL) is a rare nail dystrophy disease, and several different clinical manifestations and mutations in the phospholipase C δ 1 (PLCD1) gene have been reported. The present study reports on one Chinese family and one sporadic case of with HL. The family members exhibited an auto...

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Detalles Bibliográficos
Autores principales:	Shen, Shuzhan, Shao, Minhua, Keyal, Uma, Wang, Xiuli, Li, Ming, Zhang, Guolong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2021
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025461/ https://www.ncbi.nlm.nih.gov/pubmed/33786625 http://dx.doi.org/10.3892/mmr.2021.12052

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