E. Kinning
AuthID: R-00K-SPG
1
TITLE: Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals
AUTHORS: Kharbanda, M; Pilz, DT; Tomkins, S; Chandler, K; Saggar, A; Fryer, A; McKay, V; Louro, P ; Smith, JC; Burn, J; Kini, U; De Burca, A; FitzPatrick, DR; Kinning, E;
PUBLISHED: 2017, SOURCE: EUROPEAN JOURNAL OF MEDICAL GENETICS, VOLUME: 60, ISSUE: 2
AUTHORS: Kharbanda, M; Pilz, DT; Tomkins, S; Chandler, K; Saggar, A; Fryer, A; McKay, V; Louro, P ; Smith, JC; Burn, J; Kini, U; De Burca, A; FitzPatrick, DR; Kinning, E;
PUBLISHED: 2017, SOURCE: EUROPEAN JOURNAL OF MEDICAL GENETICS, VOLUME: 60, ISSUE: 2
