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Characterization of mutations on the rare duplicated C4/CYP21 haplotype in steroid 21-hydroxylase deficiency
Anna Wedell, Barbro Stengler, Holger LuthmanVolume:
94
Language:
english
Pages:
5
DOI:
10.1007/bf02272841
Date:
July, 1994
File:
PDF, 627 KB
english, 1994