In vitro splicing deficiency induced by a C to T mutation at position -3 in the intron 10 acceptor site of the phenylalanine hydroxylase gene in a patient with phenylketonuria
(Q72017016)
scientific article published on 01 September 1995
scientific article published on 01 September 1995
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description | scientific article published on 01 September 1995 |
External Links
(P356) |
10.1074/JBC.270.35.20370
|
(P698) |
7657610
|