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Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21.
Martinez-Thompson, Jennifer M; Niu, Zhiyv; Tracy, Jennifer A; Moore, Steven A; Swenson, Andrea; Wieben, Eric D; Milone, Margherita.
Afiliação
  • Martinez-Thompson JM; Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, Minnesota, 55905, USA.
  • Niu Z; Department of Laboratory Medicine & Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Tracy JA; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.
  • Moore SA; Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, Minnesota, 55905, USA.
  • Swenson A; Department of Pathology University of Iowa, Iowa City, Iowa, USA.
  • Wieben ED; Department of Neurology, University of Iowa, Iowa City, Iowa, USA.
  • Milone M; Department of Biochemistry & Molecular Biology, Mayo Clinic, Rochester, Minnesota, USA.
Muscle Nerve ; 57(4): 679-683, 2018 04.
Article em En | MEDLINE | ID: mdl-28881388

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Calpaína / Atrofia Muscular / Debilidade Muscular / Distrofia Muscular do Cíngulo dos Membros / Músculos Paraespinais / Proteínas Musculares Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Calpaína / Atrofia Muscular / Debilidade Muscular / Distrofia Muscular do Cíngulo dos Membros / Músculos Paraespinais / Proteínas Musculares Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article