Case Reports
doi: 10.1007/BF01799177.
Leigh syndrome due to pyruvate dehydrogenase E1 alpha deficiency (point mutation R263G) in a Spanish boy
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- PMID: 8982956
- DOI: 10.1007/BF01799177
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Case Reports
Leigh syndrome due to pyruvate dehydrogenase E1 alpha deficiency (point mutation R263G) in a Spanish boy
J Inherit Metab Dis.
1996.
No abstract available
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References
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- Hum Mutat. 1996;7(1):46-51 - PubMed
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