Case Report
Published on 20 Apr 2018
Whole Exome Sequencing Identified a Novel Heterozygous Mutation in HMBS Gene in a Chinese Patient With Acute Intermittent Porphyria With Rare Type of Mild Anemia
in Genetics of Common and Rare Diseases
![Whole Exome Sequencing Identified a Novel Heterozygous Mutation in HMBS Gene in a Chinese Patient With Acute Intermittent Porphyria With Rare Type of Mild Anemia](https://www.frontiersin.org/files/myhome article library/344976/344976_Thumb_400.jpg)
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