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Molecular Variants of Luteinizing Hormone in Three Populations of Southeast Asia

1998; Karger Publishers; Volume: 48; Issue: 4 Linguagem: Inglês

10.1159/000022807

1423-0062

Lakshmi Ramanujam, Wu-xiang Liao, A.C. Roy, Soon Chye Ng, Shan S. Ratnam,

Ovarian function and disorders

Three populations of Southeast Asia comprising 191 Chinese, 121 Malays and 150 Indians, were studied with respect to two recently described mutant luteinizing hormone (LH) variants using molecular techniques. One of these variants had Trp⁸ to Arg⁸ and Ile¹⁵ to Thr¹⁵ replacements in exon 2 of the LH β-subunit, while the other variant possessed Ser¹⁰² substitution for Gly¹⁰² in exon 3. The exon 2 mutants were in complete linkage disequilibrium. The exon 2 variant had an allele frequency of 0.045 in Chinese, 0.062 in Malays and 0.030 in Indians. The allele frequency of the exon 3 variant was 0.018 in Chinese and null in Malays and Indians. The two LH variants may be markers of interest in studies of disturbed pituitary-gonadal function, menstrual disorders and female infertility.