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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Dent disease: Same CLCN5 mutation but different phenotypes in two brothers in China

Hongwen Zhang1, Fang Wang1, Huijie Xiao1

  • 1Department of Pediatric, Peking University First Hospital, Beijing, China.

Intractable & Rare Diseases Research
|June 6, 2017
PubMed

Keywords:
CLCN5ChinaDent diseasephenotpye

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