Novel mutations in African American patients with glycogen storage disease Type II. Mutations in brief no. 209. Online.

N. Raben, E. Lee, L. Lee, R. Hirschhorn, P. H. Plotz

Research output: Contribution to journalArticle

Abstract

The infantile form of GSD II (an inherited deficiency of the lysosomal enzyme, acid alpha-glucosidase, Pompe disease) is a severe and invariably fatal disease characterized by a rapidly progressive generalized hypotonia, hepatomegaly, and cardiomegaly. We have recently demonstrated that African American patients share a common nonsense R854X mutation in exon 18 (Becker et al., 1998). Two other mutations, D645E and M519V, have been identified in individual African American patients (Hermans et al., 1993a; Huie et al., 1994a). We describe here three novel mutations in this population group: a missense W481R in exon 10, a deletion of a T1441 in exon 10, and a splicing defect at the 5' donor site of intron 8 (IVS g+la) . The splicing defect is shared by two unrelated patients and it is linked to intragenic polymorphic sites identical to those found in patients bearing the common R854X mutation.

Original languageEnglish (US)
Pages (from-to)83-84
Number of pages2
JournalHuman Mutation
Volume13
Issue number1
StatePublished - 1999
Externally publishedYes

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Glycogen Storage Disease Type II
African Americans
Exons
Mutation
Muscle Hypotonia
alpha-Glucosidases
Hepatomegaly
Nonsense Codon
Cardiomegaly
Population Groups
Introns
Tissue Donors
Acids
Enzymes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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Novel mutations in African American patients with glycogen storage disease Type II. Mutations in brief no. 209. Online. / Raben, N.; Lee, E.; Lee, L.; Hirschhorn, R.; Plotz, P. H.

In: Human Mutation, Vol. 13, No. 1, 1999, p. 83-84.

Research output: Contribution to journalArticle

Raben, N, Lee, E, Lee, L, Hirschhorn, R & Plotz, PH 1999, 'Novel mutations in African American patients with glycogen storage disease Type II. Mutations in brief no. 209. Online.', Human Mutation, vol. 13, no. 1, pp. 83-84.
Raben, N. ; Lee, E. ; Lee, L. ; Hirschhorn, R. ; Plotz, P. H. / Novel mutations in African American patients with glycogen storage disease Type II. Mutations in brief no. 209. Online. In: Human Mutation. 1999 ; Vol. 13, No. 1. pp. 83-84.
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