Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families (Q36316862)
scientific article published on July 1, 1997
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(P31) (Q13442814)
(P50) (Q98569170)
(Q28321912)
(P304) 16-22
(P407) (Q1860)
(P433) 1
(P478) 63
(P577) Tuesday, July 1, 1997
Tuesday, July 1, 1997
(P921) (Q935710)
(P953) https://jnnp.bmj.com/content/63/1/16.full.pdf
https://europepmc.org/articles/PMC2169628
https://europepmc.org/articles/PMC2169628?pdf=render
https://syndication.highwire.org/content/doi/10.1136/jnnp.63.1.16
(P1433) (Q1599804)
(P1476) "Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families" (language: en)
(P2093) G. Uziel
E. Lamantea
G. M. Fratta
E. Ciceri
F. Carrara
(P2860) (Q28252128)
(Q38477714)
(Q37891791)
(Q34627393)
(Q33208167)
(Q35199431)
(Q41275168)
(Q54655856)
(Q42512267)
(Q48450898)
(Q41559426)
(Q52226853)
(Q67900983)
(Q70472763)
(Q72632067)
(Q72437100)
(Q72092169)
(Q72792353)
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description scientific article published on July 1, 1997

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