亨特综合征
遗传学
基因
硫酸酯酶
鉴定(生物学)
生物
粘多糖病Ⅱ型
医学
计算生物学
内科学
疾病
生物化学
酶
生态学
酶替代疗法
作者
Roseline Froissart,Irène Maire,Gilles Millat,Stéphane Cudry,Anne‐Marie Birot,Véronique Bonnet,Olivier Bouton,Dominique Bozon
标识
DOI:10.1111/j.1399-0004.1998.tb02746.x
摘要
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.
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