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de Novo TINF2 C.845G>A: Pathogenic Variant in Patient with Dyskeratosis Congenita
Dyskeratosis congenita (DC) is a clinically and genetically heterogeneous, multisystem inherited syndrome with a very high risk for bone marrow failure (BMF) and cancer predisposition. The classical clinical form of DC is characterized by abnormal skin pigmentation, nail dystrophy, and oral leukopla...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Sciendo
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524180/ https://www.ncbi.nlm.nih.gov/pubmed/36249522 http://dx.doi.org/10.2478/bjmg-2021-0027 |