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PMID: 8432537 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Identification of six new Gaucher disease mutations.

Genomics ·Vol. 15 ·No. 1 ·1993-01-00 ·Pages 203-5

Beutler E, Gelbart T, West C

Abstract

The four most common mutations account for 97% of the Gaucher disease-producing alleles in Jewish patients and 75% of the alleles in non-Jewish patients. Although at least 15 other mutations and some examples of gene conversion and/or fusion genes have been described, a number of mutations remain unidentified. We have now identified six new mutations, a deletion of a C at the 72 position of the cDNA, a 481C-->T mutation (122Pro-->Ser), a 751T-->C (212Tyr-->His), a 1549G-->A (478Gly-->Ser), a 1604G-->A (496Arg-->His), and a 55-bp deletion. All but one of these were found in single families. The 1604A mutation, however, was observed in four unrelated individuals.

MeSH Terms
Adolescent Adult Base Sequence Child Child, Preschool DNA DNA Mutational Analysis Gaucher Disease/ethnology,genetics Glucosylceramidase/genetics Humans Jews/genetics Molecular Sequence Data Mutation Polymerase Chain Reaction Polymorphism, Genetic
Chemicals
DNA Glucosylceramidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Beutler E
Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, California 92037.
Gelbart T
West C
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1993-01-00
Pages
203-5
Language
English
Region
United States
NLM ID
8800135
Subset
IM
Grants
NIDDK NIH HHS · DK36639-06 · United States
NCRR NIH HHS · RR00833 · United States
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