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Twenty-Five Years of Spinal Muscular Atrophy Research: From Phenotype to Genotype to Therapy, and What Comes Next.
Wirth, Brunhilde; Karakaya, Mert; Kye, Min Jeong; Mendoza-Ferreira, Natalia.
Afiliação
  • Wirth B; Institute of Human Genetics, Center for Molecular Medicine Cologne and Center for Rare Diseases, University Hospital of Cologne, University of Cologne, 50931 Cologne, Germany; email: brunhilde.wirth@uk-koeln.de.
  • Karakaya M; Institute of Human Genetics, Center for Molecular Medicine Cologne and Center for Rare Diseases, University Hospital of Cologne, University of Cologne, 50931 Cologne, Germany; email: brunhilde.wirth@uk-koeln.de.
  • Kye MJ; Institute of Human Genetics, Center for Molecular Medicine Cologne and Center for Rare Diseases, University Hospital of Cologne, University of Cologne, 50931 Cologne, Germany; email: brunhilde.wirth@uk-koeln.de.
  • Mendoza-Ferreira N; Institute of Human Genetics, Center for Molecular Medicine Cologne and Center for Rare Diseases, University Hospital of Cologne, University of Cologne, 50931 Cologne, Germany; email: brunhilde.wirth@uk-koeln.de.
Annu Rev Genomics Hum Genet ; 21: 231-261, 2020 08 31.
Article em En | MEDLINE | ID: mdl-32004094
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Oligonucleotídeos Antissenso Limite: Animals / Humans Idioma: En Revista: Annu Rev Genomics Hum Genet Assunto da revista: GENETICA / GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Oligonucleotídeos Antissenso Limite: Animals / Humans Idioma: En Revista: Annu Rev Genomics Hum Genet Assunto da revista: GENETICA / GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article