Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency. (Q35247977)
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(P304) 511-517
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(P433) 4
(P478) 44
(P577) Saturday, April 1, 1989
(P921) (Q194041)
(P1433) (Q4744249)
(P1476) "Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency" (language: en)
(P2093) Caillaud C
Rey F
Berthelon M
Frézal J
Rey J
Munnich A
(P2860) (Q40302354)
(Q24602315)
(Q53014963)
(Q45886429)
(Q34161989)
(Q27861076)
(Q36423199)
(Q41902886)
(Q47397629)
(Q35245535)
(Q28300232)
(Q41517188)
(Q22066207)
(Q55062488)
(Q48344920)
(Q67343289)
(Q67442059)
(Q70412277)
(Q69856336)
(Q30253306)
(Q59088186)
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(Q70170462)
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