Conclusion: The result showed that terminal deletion of Xq and telomeric deletion of X chromosome were important factors of premature ovarian failure.
结论：本文的研究结果提示X染色体长臂末端可能是卵巢早衰的特异性基因区段并与X染色体末端端粒的缺失有关。
The SDCT2 with C-terminal deletion was almost entirely distributed at the basolateral membrane, nearly not expressed at the apical membrane, and seldom expressed in the cytoplasm.
端缺失的SDCT2蛋白主要位于基底侧膜上，顶膜几乎没有表达，细胞质中表达很少。
The SDCT2 with C-terminal deletion was almost entirely distributed at the basolateral membrane, nearly not expressed at the apical membrane, and seldom expressed in the cytoplasm.
端缺失的SDCT2蛋白主要位于基底侧膜上，顶膜几乎没有表达，细胞质中表达很少。
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