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Further delineation of MYO18B-related autosomal recessive Klippel-Feil syndrome with myopathy and facial dysmorphism.
Altuame, Fadie D; Haldeman-Englert, Chad; Cupler, Edward; Al Muhaizea, Mohammad A; Al-Zaidan, Hamad I; Hashem, Mais; Alkuraya, Fowzan S.
Afiliação
  • Altuame FD; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Haldeman-Englert C; Department of Medical Genetics, Mission Fullerton Genetics Center, Asheville, North Carolina, USA.
  • Cupler E; Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia.
  • Al Muhaizea MA; Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Zaidan HI; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Hashem M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Am J Med Genet A ; 185(2): 370-376, 2021 02.
Article em En | MEDLINE | ID: mdl-33179433

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Miosinas / Miopatias da Nemalina / Proteínas Supressoras de Tumor / Síndrome de Klippel-Feil / Cardiomiopatias Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Arábia Saudita

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Miosinas / Miopatias da Nemalina / Proteínas Supressoras de Tumor / Síndrome de Klippel-Feil / Cardiomiopatias Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Arábia Saudita