Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease (Q28218346)
scientific article (publication date: May 2002)
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Current Data About Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease
(P31) (Q13442814)

(P50) (Q15443108)
(P1545) 12
(P1932) Salvatore DiMauro

(Q57004101)
(P1545) 2
(P1932) Sabrina Sacconi

(P304) 862-5

(P407) (Q1860)

(P433) 5

(P478) 59

(P577) +2002-05-00T00:00:00Z

(P921) (Q2362826)
(P887)

(P1433) (Q15766672)

(P1476) "Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease" (language: en)

(P2093) Leonardo Salviati
(P1545) 1

Minerva M Rasalan
(P1545) 3

David F Kronn
(P1545) 4

Alex Braun
(P1545) 5

Peter Canoll
(P1545) 6

Mercy Davidson
(P1545) 7

Sara Shanske
(P1545) 8

Eduardo Bonilla
(P1545) 9

Arthur P Hays
(P1545) 10

Eric A Schon
(P1545) 11

other details
description scientific article (publication date: May 2002)

External Links
(P356) 10.1001/ARCHNEUR.59.5.862
(P698) 12020273