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In Silico Analysis of a De Novo OTC Variant as a Cause of Ornithine Transcarbamylase Deficiency.
Ozdemir, Yesim; Cag, Murat; Gul, Seref; Yüksel, Zafer; Ergoren, Mahmut C.
Afiliação
  • Ozdemir Y; Medical Genetics Department, Medical Faculty, Uskudar University.
  • Cag M; Generel Surgery Department, Memorial Bahcelievler Hospital, Istanbul, Turkey.
  • Gul S; Department of Chemical and Biological Engineering, Faculty of Engineering, Koc University.
  • Yüksel Z; Human Genetics, Bioscientia GmbH, Ingelheim, Germany.
  • Ergoren MC; Department of Medical Genetics, Faculty of Medicine, Near East University.
Appl Immunohistochem Mol Morphol ; 30(2): 153-156, 2022 02 01.
Article em En | MEDLINE | ID: mdl-34670952
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença da Deficiência de Ornitina Carbomoiltransferase / Hiperamonemia Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença da Deficiência de Ornitina Carbomoiltransferase / Hiperamonemia Idioma: En Ano de publicação: 2022 Tipo de documento: Article