| Literature DB >> 10738517 |
N Alif1, K Hess, J Straczek, S Sebbar, A N'Bou, P Nabet, B Dousset.
Abstract
A group of 13 Moroccan patients with MPS I and their families, including three siblings and twin siblings, was screened for mutations of the alpha-L-iduronidase gene using fluorescence-assisted mismatch analysis (FAMA) and cycle sequencing of PCR products. The P533R mutation, which is rare in Europeans, was identified in 92% of mutant alleles (24/26). This is the highest frequency of this mutation detected in patients with Hurler syndrome. None of the patients carried the W402X or Q70X alleles, the most common MPS I mutations in Europeans. These results suggest that the P533R mutation constitutes the genetic lesion which results in MPS I in people of Moroccan descent and provides yet more evidence for the uneven geographical distribution of mutations in MPS I.Entities:
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Year: 1999 PMID: 10738517 DOI: 10.1046/j.1469-1809.1999.6310009.x
Source DB: PubMed Journal: Ann Hum Genet ISSN: 0003-4800 Impact factor: 1.670