A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease (Q73131079)
scientific article published on 01 October 2000
Language:
(P31) (Q13442814)
(P304) 140-143
(P433) S 1-2
(P478) 179
(P577) Sunday, October 1, 2000
(P921) (Q117121)
(P1433) (Q6296168)
(P1476) "A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease" (language: en)
(P2093) R Majumdar
M Al Jumah
S Al Rajeh
M Fraser
A Al Zaben
A Awada
I Al Traif
M Paterson
(P2860) (Q48075338)
(Q24336948)
(Q35249090)
(Q33682273)
(Q47830547)
(Q34289999)
(Q74048061)
(Q74310623)
(Q22008012)
other details
description scientific article published on 01 October 2000

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