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.

Francis, Aneeta; George, Anuja Elizabeth; Ashok, Priya; Chandran, Reena

Francis, Aneeta; George, Anuja Elizabeth; Ashok, Priya; Chandran, Reena.

Afiliação

Francis A; Department of Dermatology & Venereology, Government Medical College, Trivandrum, India.
George AE; Department of Dermatology & Venereology, Government Medical College, Trivandrum, India.
Ashok P; Department of Dermatology & Venereology, Government Medical College, Trivandrum, India.
Chandran R; Department of Dermatology & Venereology, Government Medical College, Trivandrum, India.

Indian J Dermatol Venereol Leprol ; : 1-3, 2024 Apr 23.

Article em En | MEDLINE | ID: mdl-38841958

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article