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Complement component 4 copy number variation andCYP21A2genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

✍ Scribed by Chen, Wuyan; Xu, Zhi; Nishitani, Miki; Ryzin, Carol; McDonnell, Nazli B.; Merke, Deborah P.

Book ID: 118036532
Publisher: Springer
Year: 2012
Tongue: English
Weight: 280 KB
Volume: 131
Category: Article
ISSN: 0340-6717
DOI: 10.1007/s00439-012-1217-8

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