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
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:39
Last Modified:	09 Jun 2017 13:35
URI:	https://irep.ntu.ac.uk/id/eprint/16296

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