A novel F11 mutation in a Chinese paediatric patient with severe factor XI deficiency.

Leung, Po-Yee; Li, Chi-Kong; Cheng, Chi-Keung; Ng, Margaret H L; Chan, Nelson C N

Leung, Po-Yee; Li, Chi-Kong; Cheng, Chi-Keung; Ng, Margaret H L; Chan, Nelson C N.

Afiliación

Leung PY; Department of Paediatrics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China. Electronic address: lpy969@ha.org.hk.
Li CK; Department of Paediatrics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Cheng CK; Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Ng MHL; Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Chan NCN; Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.

Thromb Res ; 190: 89-90, 2020 06.

Article en En | MEDLINE | ID: mdl-32335422

Asunto(s)

Deficiencia del Factor XI; Niño; China; Factor XI/genética; Deficiencia del Factor XI/genética; Heterocigoto; Humanos; Mutación; Mutación Missense; Linaje

Palabras clave

F11; Factor XI deficiency; Haemophilia C; Novel mutation; Paediatric

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Deficiencia del Factor XI Límite: Child / Humans País/Región como asunto: Asia Idioma: En Revista: Thromb Res Año: 2020 Tipo del documento: Article

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