Genetics
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18 february 2020 20:00:04 |
| Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations (European Journal of Human Genetics) |
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| 179 viewsCategory: Genetics |
 Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20 (European Journal of Human Genetics)Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci (Nature Genetics) 
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