Exome-wide association study identified genetic variants contributing to the risk of cerebral palsy

Abstract excerpt

<title>Abstract</title> <p>Cerebral palsy (CP) is the most common physical disability in childhood that results from the interaction of environmental and genetic factors. Yet in many patients, the etiology remains unknown. We identified significant association at rs3131787 within the human leukocyte antigen (HLA) region using two-stage association study between 1,090 CP cases and 1,100 controls. Fine mapping of t...

Topics

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• Cerebral Palsy
• Child
• Genotype
• HLA-B Antigens
• Infant, Low Birth Weight
• Infant, Newborn
• Pregnancy
• Pregnancy Complications

Identifiers and source

Literature Corpus work

8e9f8870-6fd9-5f18-9cb2-26ed09687576

DOI

10.21203/rs.3.rs-2368855/v1