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Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene.
E Cleiren, O BĂ©nichou, E Van Hul, J Gram, J Bollerslev, F R Singer, K Beaverson, A Aledo, M P Whyte, T Yoneyama, M C deVernejoul, W Van Hul
Human Molecular Genetics 2001; 10(25):2861-2867
ICID: 830298
IC™ Value: 19.05
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