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Large-scale whole-exome sequencing association study identifies FOXH1 gene and sphingolipid metabolism pathway

Wei Zhou1,2,3,4, Luan Chen3,4, Bixuan Jiang3,4

  • 1Department of Obstetrics and Gynecology, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.

CNS Neuroscience & Therapeutics
|October 11, 2021
PubMed

Keywords:
UK biobankburden analysismajor depressive disorderrare variantswhole-exome sequencing

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