Mutation-haplotype analysis of steroid 21-hydroxylase (CYP21) deficiency in Finland. Implications for the population history of defective alleles
- 17 March 1997
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 99 (4) , 488-497
- https://doi.org/10.1007/s004390050394
Abstract
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