De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring (Q71995466)
scientific article published on 01 September 1995
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(P31) (Q13442814)
(P50) (Q5938385)
(P304) 290-294
(P433) 3
(P478) 96
(P577) Friday, September 1, 1995
(P1433) (Q5937167)
(P1476) "De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring" (language: en)
(P2093) M H Tulinius
M Houshmand
E Holme
A Oldfors
E Holmberg
J Wahlström
(P2860) (Q27860659)
(Q35696491)
(Q33208167)
(Q52226853)
(Q40678892)
(Q34627393)
(Q44795120)
(Q72607130)
(Q72357983)
(Q67927084)
(Q67583149)
(Q72632067)
other details
description scientific article published on 01 September 1995

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