一个患有先天性双行睫的家族中的非典型血清胆碱酯酶。
Atypical serum cholinesterase in a family with congenital distichiasis.
作者信息
Shammas H F, Tabbara K F, der Kaloustian V M
出版信息
J Med Genet. 1976 Dec;13(6):514-5. doi: 10.1136/jmg.13.6.514.
Abstract
This paper describes the coexistence of genetically determined reduced cholinesterase activity and congenital distichiasis in the same family. The pedigree suggests that these two autosomal dominant diseases are segregated independently and do not show evidence of linkage.
摘要
本文描述了在同一家族中遗传决定的胆碱酯酶活性降低与先天性双行睫并存的情况。系谱表明这两种常染色体显性疾病是独立分离的，且未显示出连锁的证据。
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