Identification of a frequent pseudodeficiency mutation in the fumarylacetoacetase gene, with implications for diagnosis of tyrosinemia type I (Q24672565)
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(P31) (Q13442814)
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(P433) 6
(P478) 55
(P577) Thursday, December 1, 1994
(P921) (Q1747726)
(P1433) (Q4744249)
(P1476) "Identification of a frequent pseudodeficiency mutation in the fumarylacetoacetase gene, with implications for diagnosis of tyrosinemia type I" (language: en)
(P2093) Rootwelt H
Brodtkorb E
Kvittingen EA
(P2860) (Q24672848)
(Q24670366)
(Q24601866)
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(Q28115241)
(Q28260005)
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(Q28243602)
(Q35889203)
(Q34272920)
(Q36452047)
(Q35916728)
(Q36816801)
(Q34578074)
(Q51636219)
(Q44259861)
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(Q45020563)
(Q93594580)
(Q68206907)
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(Q72165042)
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