Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene.

Dhasakeerthi, Thirumalaivasan; Aravindhan, Akilandeswari; Woodall, Aaron; Mills, Weston; Veerapandiyan, Aravindhan

Dhasakeerthi, Thirumalaivasan; Aravindhan, Akilandeswari; Woodall, Aaron; Mills, Weston; Veerapandiyan, Aravindhan.

Afiliación

Dhasakeerthi T; Departments of Neurology, University of Tennessee Health Science Center, Memphis, TN.
Aravindhan A; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR.
Woodall A; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR.
Mills W; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR.
Veerapandiyan A; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR.

J Clin Neuromuscul Dis ; 23(1): 54-55, 2021 Sep 01.

Article en En | MEDLINE | ID: mdl-34431804

Asunto(s)

Síndromes Miasténicos Congénitos; Humanos; Mutación/genética; Síndromes Miasténicos Congénitos/genética

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes Miasténicos Congénitos Límite: Humans Idioma: En Revista: J Clin Neuromuscul Dis Asunto de la revista: FISIOLOGIA / NEUROLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Túnez

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