Pathogenesis of leukodystrophy for Krabbe disease: Molecular mechanism and clinical treatment
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health
Reference13 articles.
1. Adrenomyeloneuropathy: a probable variant of adrenoleukodystrophy. II. General pathologic, neuropathologic, and biochemical aspects;Schaumburg;Neurology,1977
2. Krabbe’s globoid cell leukodystrophy: deficiency of galactocerebroside beta-galactosidase activity;Suzuki;J Neuropathol Exp Neurol,1971
3. Hereditary leucodystrophy in the mouse: the new mutant twitcher;Duchen;Brain,1980
4. Cloning and expression of cDNA encoding human galactocerebrosidase, the enzyme deficient in globoid cell leukodystrophy;Chen;Hum Mol Genet,1993
5. Krabbe disease: isolation and characterization of a full-length cDNA for human galactocerebrosidase;Sakai;Biochem Biophys Res Commun,1994
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3. Krabbe Disease–To Add or Not to Newborn Screening?;OBM Genetics;2024-01-12
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