Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians (Q24676047)
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(P31) (Q13442814)
(P304) 694-702
(P407) (Q1860)
(P433) 4
(P478) 58
(P577) Monday, April 1, 1996
(P921) (Q32137157)
(P1433) (Q4744249)
(P1476) "Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians" (language: en)
(P2093) H L Tai
E Y Krynetski
C R Yates
T Loennechen
M Y Fessing
N F Krynetskaia
W E Evans
(P2860) (Q20900776)
(Q24308648)
(Q24563229)
(Q24674721)
(Q25938986)
(Q27820693)
(Q25938983)
(Q28131648)
(Q33624061)
(Q40720516)
(Q34045219)
(Q41081740)
(Q43531554)
(Q44917795)
(Q52162405)
(Q54748250)
(Q53752011)
(Q58450543)
(Q72209986)
(Q70375962)
(Q70505455)
(Q72752612)
(Q72724778)
(Q72648752)
(Q72126155)
(Q71852856)
(Q70905277)
(Q68092294)
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