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Clinical highlights of a very rare phospolipid remodeling disease due to MBOAT7 gene defect.
Dursun, Ali; Yalnizoglu, Dilek; Özgül, Riza K; Karli Oguz, Kader; Yücel-Yilmaz, Didem.
Afiliação
  • Dursun A; Hacettepe University Faculty of Medicine, Department of Pediatric Metabolism, Ankara, Turkey.
  • Yalnizoglu D; Hacettepe University Faculty of Medicine, Department of Pediatric Neurology, Ankara, Turkey.
  • Özgül RK; Hacettepe University Institute of Child Health, Ankara, Turkey.
  • Karli Oguz K; Hacettepe University Faculty of Medicine, Department of Radiology, Ankara, Turkey.
  • Yücel-Yilmaz D; Hacettepe University Institute of Child Health, Ankara, Turkey.
Am J Med Genet B Neuropsychiatr Genet ; 183(1): 3-4, 2020 01.
Article em En | MEDLINE | ID: mdl-31512396
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiência Intelectual Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiência Intelectual Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article