| Literature DB >> 9660053 |
R Froissart1, I Maire, G Millat, S Cudry, A M Birot, V Bonnet, O Bouton, D Bozon.
Abstract
We studied 70 unrelated Hunter patients and found a gene alteration in every patient. The molecular heterogeneity was very important. Large gene rearrangements were identified in 14 patients. Forty-three different mutations were identified in the 56 other patients and 31 were not previously described. Deletions and insertions, splice site mutations were associated with a severe phenotype as nonsense mutations except Q531X. Only a few mutations were present in several patients making difficult genotype-phenotype correlations. Mutation identification allows accurate carrier detection improving prenatal diagnosis. The mother was not found to be a carrier in five cases among the 44 sporadic cases. Haplotype analysis demonstrated a higher frequency of mutations in male meiosis.Entities:
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Year: 1998 PMID: 9660053 DOI: 10.1111/j.1399-0004.1998.tb02746.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438