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Phenotypic and molecular features of Thai patients with primary carnitine deficiency.
Liammongkolkul, Somporn; Boonyawat, Boonchai; Vijarnsorn, Chodchanok; Tim-Aroon, Thipwimol; Wasant, Pornswan; Vatanavicharn, Nithiwat.
Afiliação
  • Liammongkolkul S; Division of Medical Genetics, Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Boonyawat B; Division of Medical Genetics, Department of Pediatrics, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand.
  • Vijarnsorn C; Division of Cardiology, Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Tim-Aroon T; Division of Medical Genetics, Department of Pediatrics, Faculty of Medicine Ramathbodi Hospital, Mahidol University, Bangkok, Thailand.
  • Wasant P; Division of Medical Genetics, Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Vatanavicharn N; Division of Medical Genetics, Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Pediatr Int ; 65(1): e15404, 2023 Jan.
Article em En | MEDLINE | ID: mdl-36321377
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espectrometria de Massas em Tandem / Membro 5 da Família 22 de Carreadores de Soluto / Cardiomiopatias Tipo de estudo: Prognostic_studies Limite: Female / Humans / Newborn País/Região como assunto: Asia Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espectrometria de Massas em Tandem / Membro 5 da Família 22 de Carreadores de Soluto / Cardiomiopatias Tipo de estudo: Prognostic_studies Limite: Female / Humans / Newborn País/Região como assunto: Asia Idioma: En Ano de publicação: 2023 Tipo de documento: Article