Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians.
Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians.
复制标题
硫嘌呤 S-甲基转移酶缺乏症:两个核苷酸转换定义了与白种人催化活性丧失相关的最常见的突变等位基因。
DOI:
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发表时间:
1996
影响因子:
9.8
通讯作者:
Evans,WE
中科院分区:
文献类型:
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作者:
Tai,HL;Krynetski,EY;Yates,CR;Loennechen,T;Fessing,MY;Krynetskaia,NF;Evans,WE
影响因子:
5.2
作者:
LENNARD, L;GIBSON, BES;LILLEYMAN, JS
通讯作者:
LILLEYMAN, JS
DOI:
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发表时间:
1978
期刊:
Clinica chimica acta; international journal of clinical chemistry
影响因子:
--
作者:
R. Weinshilboum;F. Raymond;P. Pazmiño
通讯作者:
P. Pazmiño