Follicle-stimulating hormone receptor gene mutations are rare in Japanese women with premature ovarian failure and polycystic ovary syndrome Kenji Takakura,

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Follicle-stimulating hormone receptor gene mutations are rare in Japanese women with premature ovarian failure and polycystic ovary syndrome Kenji Takakura, M.D., Koichi Takebayashi, M.D., Hua-Qin Wang, M.D., Fuminori Kimura, M.D., Kyoko Kasahara, M.D., Yoichi Noda, M.D. Fertility and Sterility Volume 75, Issue 1, Pages 207-209 (January 2001) DOI: 10.1016/S0015-0282(00)01673-3

Figure 1 Representative polyacrylamide gel electrophoresis for FSH receptor exon 6 (lanes 1 and 2), 7 (lanes 3 and 4), and 10 (lanes 5 and 6). Lanes 1, 3, and 5 are uncut DNA used only to illustrate the size of a mutant allele (101, 86, and 216 bp, respectively), as no mutant alleles were observed. Lanes 2, 4, and 6 are representative of patients’ DNA digested completely with restriction enzymes MunI, BsmI, and HhaI, respectively. The molecular weight marker ladder is shown in lane M. Takakura. FSH receptor gene mutations. Fertil Steril 2001. Fertility and Sterility 2001 75, 207-209DOI: (10.1016/S0015-0282(00)01673-3)