Enhanced proteasomal degradation of mutant human thiopurine S-methyltransferase (TPMT) in mammalian cells: mechanism for TPMT protein deficiency inherited by TPMT*2, TPMT*3A, TPMT*3B or TPMT*3C.

Source:http://linkedlifedata.com/resource/pubmed/id/10591545

Download in:

View as

General Info

PMID
10591545