Apparent biochemical homozygosity in two obligatory heterozygotes for metachromatic leukodystrophy. | J Pediatr;89(3): 438-40, 1976 Sep. | MEDLINE

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Apparent biochemical homozygosity in two obligatory heterozygotes for metachromatic leukodystrophy.

Lott, I T; Dulaney, J T; Milunsky, A; Hoefnagel, D; Moser, H W.

J Pediatr ; 89(3): 438-40, 1976 Sep.

Article in En | MEDLINE | ID: mdl-8599

Subject(s)

Cerebroside-Sulfatase/metabolism; Hexosaminidases/metabolism; Leukodystrophy, Metachromatic/enzymology; Sulfatases/metabolism; Child, Preschool; Heterozygote; Homozygote; Humans; Sulfoglycosphingolipids/urine

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Collection: 01-internacional Database: MEDLINE Main subject: Sulfatases / Cerebroside-Sulfatase / Hexosaminidases / Leukodystrophy, Metachromatic Limits: Child, preschool / Humans Language: En Journal: J Pediatr Year: 1976 Document type: Article Country of publication: United States

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Collection: 01-internacional Database: MEDLINE Main subject: Sulfatases / Cerebroside-Sulfatase / Hexosaminidases / Leukodystrophy, Metachromatic Limits: Child, preschool / Humans Language: En Journal: J Pediatr Year: 1976 Document type: Article Country of publication: United States