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A genetic analysis of the Papillon-Lefèvre syndrome in a Jewish family from Cochin.

作者信息

Hacham-Zadeh S, Schaap T, Cohen M M

出版信息

Am J Med Genet. 1978;2(2):153-7. doi: 10.1002/ajmg.1320020206.

DOI:10.1002/ajmg.1320020206
PMID:162525
Abstract

The Papillon-Lefèvre syndrome (PLS) is segregating in a large kindred of a Jewish isolate originating from Cochin, India. The frequency of the gene responsible for PLS among the Cochin Jews, 0.1, was estimated from the number of unrelated carriers in the isolate who married into the kindred. The obvious discrepancy between this apparently high gene frequency and the total absence of PLS in other kindreds of the isolate suggests that the syndrome may not behave as a simple autosomal recessive trait.

摘要

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引用本文的文献

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Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C.海姆-蒙克综合征和帕皮永-勒费弗尔综合征是组织蛋白酶C的等位基因突变。
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