Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation (Q34536343)
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Current Data About Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation
(P31) (Q13442814)
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(P50) (Q37359439)
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(P1932) Konrad Oexle

(Q28354352)
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(P1932) Andrea Superti-Furga

(Q87140180)
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(P1932) Lambert van den Heuvel
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(Q62560469)
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(P1932) Jan Smeitink
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(P1476) "Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation" (language: en)
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(P2093) Olga Grafakou
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Roel Smeets
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Frans Trijbels
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Hans H Goebel
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Nils Bosshard
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Beat Steinmann
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External Links
(P356) 10.1007/S00431-003-1282-Z
(P698) 12925875
(P5875) 10607738
(P6179) 1031478404