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Two novel missense mutations in the cystathionine beta-synthase gene in homocystinuric patients.

Authors :
Kluijtmans LA
Blom HJ
Boers GH
van Oost BA
Trijbels FJ
van den Heuvel LP
Source :
Human genetics [Hum Genet] 1995 Aug; Vol. 96 (2), pp. 249-50.
Publication Year :
1995

Abstract

Direct sequencing of the coding region of the cystathionine beta-synthase (CBS) gene in two homocystinuric patients revealed the presence of two novel missense mutations. The first mutation, a 1111G-->A transition, resulted in the substitution of the evolutionary conserved valine-371 by a methionine residue (V371M) and created a new NlaIII restriction site. The second mutation, a G-->A transition at base-pair 494, resulted in an amino acid change from cysteine to tyrosine (C165Y) and abolished a BsoFI restriction site. Both mutations were found in a compound heterozygous state with the previously described 833T-->C transition.

Details

Language :
English
ISSN :
0340-6717
Volume :
96
Issue :
2
Database :
MEDLINE
Journal :
Human genetics
Publication Type :
Academic Journal
Accession number :
7635485
Full Text :
https://doi.org/10.1007/BF00207394