The genotype and allele frequency of SNP rs35874463 and rs17228212 in 372 CHD patients and 456 non-CHD controls.

Name: The genotype and allele frequency of SNP rs35874463 and rs17228212 in 372 CHD patients and 456 non-CHD controls.
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NIAID Data Ecosystem2026-03-08 收录

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https://figshare.com/articles/dataset/_Characterization_of_SMAD3_Gene_Variants_for_Possible_Roles_in_Ventricular_Septal_Defects_and_Other_Congenital_Heart_Diseases_/1464707

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2015-06-25