Fujimoto A.; Kurban M.; Nakamura M.; Farooq M.; Fujikawa H.; Kibbi A.-G.; Ito M.; Dahdah M.; Matta M.; Diab H.; Shimomura Y.
(CLAREELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000, IRELAND, 2013)
Background: Clouston syndrome is a rare autosomal dominant condition characterized by hypotrichosis, nail dystrophy, and occasionally palmoplantar keratoderma. The disease is caused by mutations in GJB6 gene, which encodes ...