Albers-Schonberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene
Year: 2001
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
Authors: E. Cleiren, O Bénichou, 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
Institution: University of Antwerp
Language: English
Topic: Bone Metabolism and Diseases
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
Funder: Army Research Office
OpenAlex ID: W2148797695