CYLD cutaneous syndrome is a genetic issue characterised by the growth of various noncancerous (benign) skin tumors. These tumors produce...
Genetics
Behne MJ, Tu CL, Aronchik I, Epstein E, Bench G, Bikle DD, Pozzan T, Mauro TM. Human keratinocyte ATP2C1 localizes...
Maturity-onset diabetes of the younger (MODY) is a team of quite a few circumstances characterised by abnormally superior blood sugar...
Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda...
Aliefendioğlu D, Tana Aslan Ay, Coşkun T, Dursun A, Cakmak FN, Kesimer M. Transient nonketotic hyperglycinemia: two case experiences and...
Campiglio M, Flucher BE. STAC3 stably interacts by means of its C1 domain with Ca(V)one.one in skeletal muscle mass triads....
Autosomal dominant partial epilepsy with auditory features (ADPEAF) is an unusual variety of epilepsy that operates in people. This dysfunction...
Chen Q, Boeve BF, Senjem M, Tosakulwong N, Lesnick T, Brushaber D, Dheel C, Fields J, Forsberg L, Gavrilova R,...
