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Leigh syndrome due to pyruvate dehydrogenase E1α deficiency (point mutation R263G) in a Spanish boy

✍ Scribed by P. Briones; M. J. López; L. De Meirleir; A. Ribes; M. Rodés; C. Martinez-Costa; M. Peris; W. Lissens


Publisher
Springer
Year
1996
Tongue
English
Weight
167 KB
Volume
19
Category
Article
ISSN
0141-8955

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