Albers-Schonberg disease

Cleiren, E., Benichou, 0., VanHul, E., Gram, J., Bollerslev, J., Singer, F.R., Beaverson, K., Aledo, A., Whyte, M.P., Yoneyama, T., deVernejoul, M.C., and VanHul, W. (2001) Albers-Schonberg Disease (Autosomal Dominant Osteopetrosis type II) Results from Mutations in the C1CN7 Chloride Chaimel Gene. Human and Molecular Genetics 10, 2861-2867. 

Cleiren E, Benichou O, Van Hul E, Gram J, Bollerslev J, Singer FR, Beaverson K, Aledo A, Whyte MP, Yoneyama T, deVemejoul MC, Van Hul W. 2001. Albers-Schonberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the C1CN7 chloride channel gene. Hum Mol Genet 10 2861-7. 

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See also in sourсe #XX -- [ ]

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