Whole-exome study to identify the causative germline mutations of congenital macrothrombocytopenia
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https://www.omicsdi.org/dataset/ega/EGAS00001000371
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资源简介：
To identify the causative germline mutations of congenital macrothrombocytopenia, whole-exome study of 6 families (21 individuals) with autosomal dominant mode of transmission.EGA study EGAS00001000371
创建时间：
2016-04-11
