Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation (Q63256322)
scientific article published on 15 February 2007
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(P577) Thursday, February 15, 2007
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(P1476) "Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation" (language: en)
(P2093) R Spiegel
A Shaag
A Gutman
S H Korman
O Elpeleg
S A Shalev
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description scientific article published on 15 February 2007

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