A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency (Q22253915)
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Current Data About A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency
(P31) (Q13442814)

(P50) (Q2863363)
(P1545) 9
(P1932) A Munnich
(P9687) A
(P9688) Munnich
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

(P304) 1245-9

(P407) (Q1860)

(P433) 8

(P478) 9

(P577) Monday, May 1, 2000

(P921) (Q21100866)
(P248)

(Q912751)
(P248)

(P1433) (Q2720965)

(P1476) "A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency" (language: en)

(P2093) I Valnot
(P1545) 1
(P9687) I
(P9688) Valnot
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

J C von Kleist-Retzow
(P1545) 2
(P9687) J C
(P9688) von Kleist-Retzow
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

A Barrientos
(P1545) 3
(P9687) A
(P9688) Barrientos
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

M Gorbatyuk
(P1545) 4
(P9687) M
(P9688) Gorbatyuk
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

J W Taanman
(P1545) 5
(P9687) J W
(P9688) Taanman
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

B Mehaye
(P1545) 6
(P9687) B
(P9688) Mehaye
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

P Rustin
(P1545) 7
(P9687) P
(P9688) Rustin
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

A Tzagoloff
(P1545) 8
(P9687) A
(P9688) Tzagoloff
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

A Rötig
(P1545) 10
(P9687) A
(P9688) Rötig
(P248)
(P698) 10767350
(P813) Wednesday, February 8, 2023

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External Links
(P356) 10.1093/HMG/9.8.1245
(P698) 10767350
(P3181) 3248506
(P5875) 12549899