Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity
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https://www.omicsdi.org/dataset/ega/EGAS00001000878
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We performed SNP and copy number variation (CNV) association analyses in 1,509 children with obesity at the extreme tail (>3 s.d. from the mean) of the BMI distribution and 5,380 controls. The control samples were made available from the EGA with accession numbers EGAD00000000021 and EGAD00000000023.EGA study EGAS00001000878
创建时间:
2014-09-16



