| Literature DB >> 7923859 |
L Lacerda1, O Amaral, R Pinto, P Oliveira, J Aerts, M C Sá Miranda.
Abstract
In the Portuguese population the most frequent form of Gaucher disease is type 1. The N370S glucocerebrosidase gene mutation accounts for 63% of mutated alleles. The frequency of this mutation was accurately determined in the Portuguese population, which does not present an Ashkenazi Jewish genetic background. A gene frequency of 0.0043, with 95% confidence limits between 0.0023 and 0.0063, was obtained studying the genomic DNA of 2000 blood cards randomly sampled from the national neonatal screening program. On the basis of this frequency a significantly high number of homozygotes for the N370S mutation should be expected in the Portuguese population. This finding supports the idea that the majority of homozygotes for this mutation present a very mild clinical phenotype and remain undiagnosed.Entities:
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Year: 1994 PMID: 7923859 DOI: 10.1111/j.1399-0004.1994.tb04034.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438