Referenced in: none

Automatically associated channels: ClC4 , ClC7

Title: A newly described mutation of the CLCN7 gene causes neuropathic autosomal recessive osteopetrosis in an Arab family.

Authors: Jumana Y Al-Aama, Amal A Dabbagh, Alaa Y Edrees

Journal, date & volume: Clin. Dysmorphol., 2012 Jan , 21, 1-7

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/21946807

Abstract