Ornithine carbamoyltransferase deficiency: molecular characterization of 29 families

Storkanova, G, Vlaskova, H, Chuzhanova, N ORCID logoORCID: https://orcid.org/0000-0002-4655-3618, Zeman, J, Stranecky, V, Majer, F, Peskova, K, Luksan, O, Jirsa, M, Hrebicek, M and Dvorakova, L, 2013. Ornithine carbamoyltransferase deficiency: molecular characterization of 29 families. Clinical Genetics.

Full text not available from this repository.
Item Type: Journal article
Publication Title: Clinical Genetics
Creators: Storkanova, G., Vlaskova, H., Chuzhanova, N., Zeman, J., Stranecky, V., Majer, F., Peskova, K., Luksan, O., Jirsa, M., Hrebicek, M. and Dvorakova, L.
Date: 2013
Identifiers:
Number
Type
10.1111/cge.12085
DOI
Divisions: Schools > School of Science and Technology
Record created by: EPrints Services
Date Added: 09 Oct 2015 10:49
Last Modified: 09 Jun 2017 13:40
URI: https://irep.ntu.ac.uk/id/eprint/18615

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