Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation

Author: Spiegel R.   Shaag A.   Gutman A.   Korman S.   Saada A.   Elpeleg O.   Shalev S.  

Publisher: Springer Publishing Company

ISSN: 0141-8955

Source: Journal of Inherited Metabolic Disease, Vol.30, Iss.2, 2007-04, pp. : 266-266

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