Novel A219P Mutation of Hydroxymethylbilane Synthase...

Novel A219P Mutation of Hydroxymethylbilane Synthase Identified in a Chinese Woman with Acute Intermittent Porphyria and Syndrome of Inappropriate Antidiuretic Hormone

Li, Yingjie, Qu, Hua, Wang, Hang, Deng, Huacong, Liu, Ziyan
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Volume:
79
Language:
english
Journal:
Annals of Human Genetics
DOI:
10.1111/ahg.12107
Date:
July, 2015
File:
PDF, 96 KB
english, 2015
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