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MAP2 - A Candidate Gene for Epilepsy, Developmental Delay and Behavioral Abnormalities in a Patient With Microdeletion 2q34.
Westphal, Dominik S; Andres, Stephanie; Makowski, Christine; Meitinger, Thomas; Hoefele, Julia.
Afiliação
  • Westphal DS; Institute of Human Genetics, Technical University of Munich, Munich, Germany.
  • Andres S; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
  • Makowski C; Institute of Human Genetics, Technical University of Munich, Munich, Germany.
  • Meitinger T; Department of Pediatrics, Technical University of Munich, Munich, Germany.
  • Hoefele J; Institute of Human Genetics, Technical University of Munich, Munich, Germany.
Front Genet ; 9: 99, 2018.
Article em En | MEDLINE | ID: mdl-29632546
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article