A closer look at ARSA activity in a patient with metachromatic leukodystrophy.

Doherty, Kathleen; Frazier, S Barron; Clark, Matthew; Childers, Anna; Pruthi, Sumit; Wenger, David A; Duis, Jessica

Doherty, Kathleen; Frazier, S Barron; Clark, Matthew; Childers, Anna; Pruthi, Sumit; Wenger, David A; Duis, Jessica.

Afiliación

Doherty K; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
Frazier SB; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
Clark M; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
Childers A; Department of Pediatrics, Division of Medical Genetics & Genomic Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Pruthi S; Department of Pediatrics, Division of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN, USA.
Wenger DA; Department of Neurology, Thomas Jefferson University, Philadelphia, PA, USA.
Duis J; Department of Pediatrics, Division of Medical Genetics & Genomic Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.

Mol Genet Metab Rep ; 19: 100460, 2019 Jun.

Article en En | MEDLINE | ID: mdl-30828547

Palabras clave

Arylsulfatase A; Inborn error of metabolism; Leukodystrophy; Lysosomal storage disease; Metachromatic Leukodystrophy

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Genet Metab Rep Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

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