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.
Full text not available from this repository.Item Type: | Journal article |
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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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