错义突变
遗传学
突变
基因型
基因
生物
疾病
表型
粘多糖病
基因突变
医学
病理
生物化学
作者
Paola Di Natale,G. Villani,Carmela Di Domenico,Aurora Daniele,Carlo Dionisi‐Vici,Andrea Bartuli
标识
DOI:10.1034/j.1399-0004.2003.00053.x
摘要
Mucopolysaccharidosis type IIIA, also known as Sanfilippo A disease, results from mutations in the sulfamidase gene. To date, a total of 62 mutations have been described underlying this lysosomal disorder. Expression studies on missense mutations have shown that each alteration was disease‐causing and helped to clarify the genotype–phenotype correlation. In this report we describe a large pedigree where the mutations have been identified in two second cousins: one with severe disease (E369K/R433Q) and the other with a mild form of the illness (E369K/P128L). This study places R433Q as a severe mutation underlying Sanfilippo A disease.
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