Infantile-Onset Complex Hereditary Spastic Paraplegia Due to a Novel Mutation in SPAST Gene.

ElSheikh, Reem H; Aravindhan, Akilandeswari; Boysen, Sebastian; Veerapandiyan, Aravindhan

ElSheikh, Reem H; Aravindhan, Akilandeswari; Boysen, Sebastian; Veerapandiyan, Aravindhan.

Afiliação

ElSheikh RH; Division of Neurology, Department of Pediatrics, University of Arkansas for Medical Sciences, Arkansas Children's Hospital, Little Rock, Arkansas.
Aravindhan A; Division of Neurology, Department of Pediatrics, University of Arkansas for Medical Sciences, Arkansas Children's Hospital, Little Rock, Arkansas.
Boysen S; Division of Neurology, Department of Pediatrics, University of Arkansas for Medical Sciences, Arkansas Children's Hospital, Little Rock, Arkansas.
Veerapandiyan A; Division of Neurology, Department of Pediatrics, University of Arkansas for Medical Sciences, Arkansas Children's Hospital, Little Rock, Arkansas. Electronic address: aveerapandiyan@uams.edu.

Pediatr Neurol ; 134: 71, 2022 09.

Article em En | MEDLINE | ID: mdl-35841713

Assuntos

Paraplegia Espástica Hereditária; Adenosina Trifosfatases; Humanos; Mutação/genética; Linhagem; Paraplegia Espástica Hereditária/genética; Espastina/genética

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária Limite: Humans Idioma: En Revista: Pediatr Neurol Ano de publicação: 2022 Tipo de documento: Article

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