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SCN10A variants associated with congenital harlequin syndrome.
Halle, Aurelie; De Becdelievre, Alix; Funalot, Benoit; Labrèze, Christine; Morice-Picard, Fanny; Boralevi, Franck.
Afiliación
  • Halle A; Department of Dermatology, Centre Hospitalier Universitaire d'Amiens, Amiens, France.
  • De Becdelievre A; Department of Medical Genetics, Henri Mondor University Hospital, AP-HP, INSERM, IMRB, Paris Est Créteil University, Créteil, France.
  • Funalot B; Department of Medical Genetics, Henri Mondor University Hospital, AP-HP, INSERM, IMRB, Paris Est Créteil University, Créteil, France.
  • Labrèze C; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Hôpital des Enfants Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
  • Morice-Picard F; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Hôpital des Enfants Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
  • Boralevi F; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Hôpital des Enfants Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Br J Dermatol ; 186(6): 1039-1041, 2022 06.
Article en En | MEDLINE | ID: mdl-35007332
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades del Sistema Nervioso Autónomo / Hipohidrosis Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades del Sistema Nervioso Autónomo / Hipohidrosis Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article