Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations

Verderio, E ORCID: https://orcid.org/0000-0001-9153-8997, Cavadini, P, Montermini, L, Wang, H, Lamantea, E, Finocchiaro, G, DiDonato, S, Gellera, C and Taroni, F, 1995. Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations. Human Molecular Genetics, 4, pp. 19-29.

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Item Type:	Journal article
Publication Title:	Human Molecular Genetics
Creators:	Verderio, E., Cavadini, P., Montermini, L., Wang, H., Lamantea, E., Finocchiaro, G., DiDonato, S., Gellera, C. and Taroni, F.
Date:	1995
Volume:	4
Divisions:	Schools > School of Science and Technology
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:08
Last Modified:	09 Jun 2017 13:20
URI:	https://irep.ntu.ac.uk/id/eprint/8372

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