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STAC3 related congenital myopathy: A case series of seven Comorian patients.
Gromand, Marie; Gueguen, Paul; Pervillé, Anne; Ferroul, Fanny; Morel, Godelieve; Harouna, Anrifati; Doray, Bérénice; Urtizberea, J Andoni; Alessandri, Jean-Luc; Robin, Stéphanie.
Afiliação
  • Gromand M; Department of Pediatrics, University Hospital Félix Guyon, La Réunion, France.
  • Gueguen P; Department of Medical Genetics, University Hospital Félix Guyon, La Réunion, France.
  • Pervillé A; Children Hospital, St Denis, La Réunion, France.
  • Ferroul F; Department of Medical Genetics, University Hospital Félix Guyon, La Réunion, France.
  • Morel G; Department of Medical Genetics, University Hospital Félix Guyon, La Réunion, France.
  • Harouna A; Department of Gynecology, Mamoudzou Hospital, Mayotte, France.
  • Doray B; Department of Medical Genetics, University Hospital Félix Guyon, La Réunion, France.
  • Urtizberea JA; Centre de Compétence Neuromusculaire, FILNEMUS, Hôpital Marin, Hendaye, France.
  • Alessandri JL; Department of Medical Genetics, University Hospital Félix Guyon, La Réunion, France. Electronic address: jean-luc.alessandri@chu-reunion.fr.
  • Robin S; Department of Pediatrics, University Hospital Félix Guyon, La Réunion, France.
Eur J Med Genet ; 65(10): 104598, 2022 Oct.
Article em En | MEDLINE | ID: mdl-36030003

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipertermia Maligna / Doenças Musculares / Miotonia Congênita Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipertermia Maligna / Doenças Musculares / Miotonia Congênita Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França