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Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype

โœ Scribed by E. P. Treacy; A. Lee-Chong; G. Roche; B. Lynch; S. Ryan; S. Goodman

Book ID
111539188
Publisher
Springer
Year
2003
Tongue
English
Weight
46 KB
Volume
26
Category
Article
ISSN
0141-8955

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