Farooq M.; Moustafa R.M.; Fujimoto A.; Fujikawa H.; Abbas O.; Kibbi A.G.; Kurban M.; Shimomura Y.
(BASELALLSCHWILERSTRASSE 10, CH-4009 BASEL, SWITZERLAND, 2012)
Background: H syndrome is a rare autosomal recessive genetic disorder which involves the skin and other systemic organs and is caused by mutations in the SLC29A3 gene. Objectives: To disclose the molecular basis of H ...