Human Genome Epidemiology Literature Finder
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| Query Trace: Disease Susceptibility and CYP21A2[original query] |
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| Complement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Human genetics 2012 Dec 131 (12): 1889-94. Chen Wuyan, Xu Zhi, Nishitani Miki, Van Ryzin Carol, McDonnell Nazli B, Merke Deborah |
- Page last reviewed:Feb 1, 2024
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