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Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II

✍ Scribed by Casper L Jessen; Jane H Christensen; Niels H Birkebæk; Soren Rittig


Book ID
117963775
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
567 KB
Volume
101
Category
Article
ISSN
0803-5253

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