Recurrent inversion with concomitant deletion and insertion events in the coagulation factor VIII gene suggests a new mechanism for X-chromosomal rearrangements causing hemophilia A

Mühle, C., Zenker, M., Chuzhanova, N. ORCID: 0000-0002-4655-3618 and Schneider, H., 2007. Recurrent inversion with concomitant deletion and insertion events in the coagulation factor VIII gene suggests a new mechanism for X-chromosomal rearrangements causing hemophilia A. Human Mutation, 28, p. 1045.

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Item Type: Journal article
Publication Title: Human Mutation
Creators: Mühle, C., Zenker, M., Chuzhanova, N. and Schneider, H.
Date: 2007
Volume: 28
Divisions: Schools > School of Science and Technology
Depositing User: EPrints Services
Date Added: 09 Oct 2015 10:39
Last Modified: 09 Jun 2017 13:35
URI: http://irep.ntu.ac.uk/id/eprint/16296

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