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Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report.
Lyahyai, Jaber; Bencheikh, Bouchra Ouled Amar; Elalaoui, Siham C; Mansouri, Maria; Boualla, Lamia; DIonne-Laporte, Alexandre; Spiegelman, Dan; Dion, Patrick A; Cossette, Patrick; Rouleau, Guy A; Sefiani, Abdelaziz.
Afiliação
  • Lyahyai J; Centre de Génomique Humaine, Faculté de Médecine et Pharmacie, Mohammed V University in Rabat, Rabat, Morocco. jaber.lyahyai@gmail.com.
  • Bencheikh BOA; Montreal Neurological Institute and Hospital, Montreal, Quebec, Canada.
  • Elalaoui SC; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
  • Mansouri M; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
  • Boualla L; Centre de Génomique Humaine, Faculté de Médecine et Pharmacie, Mohammed V University in Rabat, Rabat, Morocco.
  • DIonne-Laporte A; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
  • Spiegelman D; Centre de Génomique Humaine, Faculté de Médecine et Pharmacie, Mohammed V University in Rabat, Rabat, Morocco.
  • Dion PA; Montreal Neurological Institute and Hospital, Montreal, Quebec, Canada.
  • Cossette P; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
  • Rouleau GA; Montreal Neurological Institute and Hospital, Montreal, Quebec, Canada.
  • Sefiani A; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
BMC Pediatr ; 18(1): 138, 2018 04 17.
Article em En | MEDLINE | ID: mdl-29665810

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BMC Pediatr Assunto da revista: PEDIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Marrocos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BMC Pediatr Assunto da revista: PEDIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Marrocos