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

VERDERIO, E., 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.

Full text not available from this repository.
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
Depositing User: EPrints Services
Date Added: 09 Oct 2015 10:08
Last Modified: 09 Jun 2017 13:20
URI: http://irep.ntu.ac.uk/id/eprint/8372

Actions (login required)

Edit View Edit View

Views

Views per month over past year

Downloads

Downloads per month over past year