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A novel homozygous missense mutation in exon 3 at codon 42 c.125G>A (p.Arg42His) in the PROC gene causing protein C deficiency and presenting as neonatal purpura fulminans

Indian Journal of Dermatology, Venereology and Leprology Pub Date : 2024-04-23 DOI:10.25259/ijdvl_618_2023
Aneeta Francis, A. George, Priya Ashok, R. Chandran
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PROC 基因第 3 外显子第 42 密码子 c.125G>A (p.Arg42His) 的新型同卵错义突变导致蛋白 C 缺乏症，并表现为新生儿白斑性紫癜
本文章由计算机程序翻译，如有差异，请以英文原文为准。
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Indian Journal of Dermatology, Venereology and Leprology
Indian Journal of Dermatology, Venereology and Leprology
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