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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
D.A. Spandidos
2021
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| Materias: | |
| 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 |