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

TARONI, F., VERDERIO, E., 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.

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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
Depositing User: EPrints Services
Date Added: 09 Oct 2015 10:48
Last Modified: 09 Jun 2017 13:39
URI: http://irep.ntu.ac.uk/id/eprint/18385

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