[A novel homozygous mutation p.E25X in the HSD3B2 gene causing salt wasting 3β-hydroxysteroid dehydrogenases deficiency in a Chinese pubertal girl: a delayed diagnosis until recurrent ovary cysts].

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Published in Zhonghua Er Ke Za Zhi on December 01, 2014

Authors

Yonglan Huang1, Jipeng Zheng, Ting Xie, Qing Xiao, Shaomei Lu, Xiuzhen Li, Jing Cheng, Lihe Chen, Li Liu

Author Affiliations

1: Department of Genetics and Endocrinology, Guangzhou Women and Children's Medical Center, Guangzhou 510623, China.

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