Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2

Jones, ML; Murden, SL; Brooks, C; Maloney, V; Manning, RA; Gilmour, KC; Bharadwaj, V; de la Fuente, J; Chakravorty, S; Mumford, AD

doi:http://dx.doi.org/10.1186/1471-2350-14-42

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Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2..pdf (441.52 KB)

Published version

Author(s)

Jones, ML

Murden, SL

Brooks, C

Maloney, V

Manning, RA

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Type

Journal Article

Date Issued

2013-04-04

URI

http://hdl.handle.net/10044/1/18793

DOI

http://dx.doi.org/10.1186/1471-2350-14-42

ISSN

1471-2350

Publisher

BIOMED CENTRAL LTD

Journal / Book Title

BMC MEDICAL GENETICS

Volume

14

Copyright Statement

© 2013 Jones et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative
Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and
reproduction in any medium, provided the original work is properly cited.

License URL

https://creativecommons.org/licenses/by/2.0/

Description

19/01/15 meb. OA paper, ok to add.

Identifier

http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000319444700001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202

ARTN 42

Publication Status

Published