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Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutations

✍ Scribed by Georgirene D. Vladutiu; Elizabeth J. Quackenbush; Bryan E. Hainline; Simone Albers; David S. Smail; Michael J. Bennett


Book ID
117848237
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
84 KB
Volume
141
Category
Article
ISSN
1097-6833

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