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Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations.
Maselli, Ricardo A; Wei, David T; Hodgson, Trent S; Sampson, Jacinda B; Vazquez, Jessica; Smith, Heather L; Pytel, Peter; Ferns, Michael.
Afiliación
  • Maselli RA; Department of Neurology, University of California Davis, Sacramento, California, USA.
  • Wei DT; Department of Neurology, University of California Davis, Sacramento, California, USA.
  • Hodgson TS; Kaiser Permanente Oakland Medical Center, Oakland, California, USA.
  • Sampson JB; Department of Neurology, Stanford University, Palo Alto, California, USA.
  • Vazquez J; Department of Neurology, University of California Davis, Sacramento, California, USA.
  • Smith HL; Department of Pathology, The University of Chicago, Chicago, Illinois, USA.
  • Pytel P; Department of Pathology, The University of Chicago, Chicago, Illinois, USA.
  • Ferns M; Department of Anesthesiology, University of California Davis, Davis, California, USA.
Muscle Nerve ; 64(2): 219-224, 2021 08.
Article en En | MEDLINE | ID: mdl-34037996
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Texto completo: 1 Colección: 01-internacional Asunto principal: Síndromes Miasténicos Congénitos / Sinaptotagmina II / Mutación / Unión Neuromuscular Tipo de estudio: Diagnostic_studies Límite: Adult / Child, preschool / Female / Humans / Male Idioma: En Revista: Muscle Nerve Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Asunto principal: Síndromes Miasténicos Congénitos / Sinaptotagmina II / Mutación / Unión Neuromuscular Tipo de estudio: Diagnostic_studies Límite: Adult / Child, preschool / Female / Humans / Male Idioma: En Revista: Muscle Nerve Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos