Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter (Q22009988)
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(P31) (Q13442814)
(P304) 151-8
(P407) (Q1860)
(P433) 2
(P478) 22
(P577) +1999-06-00T00:00:00Z
(P921) (Q39572)
(P1433) (Q976454)
(P1476) "Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter" (language: en)
(P2093) J A Camacho
C Obie
B Biery
B K Goodman
C A Hu
S Almashanu
G Steel
R Casey
M Lambert
G A Mitchell
D Valle
(P2860) (Q71238616)
(Q68213108)
(Q42007417)
(Q72364824)
(Q47874172)
(Q52229458)
(Q41981517)
(Q73785194)
(Q70979953)
(Q28254861)
(Q27931655)
(Q56990020)
(Q41022479)
(Q48034687)
(Q27930085)
(Q27930377)
(Q24311431)
(Q77219242)
(Q28115954)
(Q70185681)
(Q24642530)
(Q32123139)
(Q52099260)
(Q36544618)
(Q22008608)
(Q42208419)
(Q39934361)
(Q42229961)
(Q68039029)
(Q58850960)
(Q58586230)
(Q53744579)
(Q24308826)
(Q60662723)
(Q28573189)
(Q52009075)
(Q70485844)
(Q68917020)
(Q33866097)
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