Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients.

Tools

Taroni, F., Verderio, E. ORCID: 0000-0001-9153-8997, Dworzak, F., Willems, P.J., Cavadini, P. and DiDonato, S., 1993. Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients. Nature Genetics, 4, pp. 314-320.

Full text not available from this repository.

Item Type:	Journal article
Publication Title:	Nature Genetics
Creators:	Taroni, F., Verderio, E., Dworzak, F., Willems, P.J., Cavadini, P. and DiDonato, S.
Date:	1993
Volume:	4
Divisions:	Schools > School of Science and Technology
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:48
Last Modified:	09 Jun 2017 13:39
URI:	https://irep.ntu.ac.uk/id/eprint/18385