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Clinical and laboratory features of seven British kindreds with hereditary hyperferritinaemia cataract syndrome

Clinical and laboratory features of seven British kindreds with hereditary hyperferritinaemia cataract syndrome
Clinical and laboratory features of seven British kindreds with hereditary hyperferritinaemia cataract syndrome
0007-1048
p.33
Siddiq, S.
3f8d958e-ce63-44d2-9180-f7b51751058b
Bower, K.
46595934-802b-47c9-b5dc-27a5f316634a
Temple, K.
d63e7c66-9fb0-46c8-855d-ee2607e6c226
Mumford, A.D.
e874dcc4-7a3e-49a7-9c4c-461169f3bb39
Siddiq, S.
3f8d958e-ce63-44d2-9180-f7b51751058b
Bower, K.
46595934-802b-47c9-b5dc-27a5f316634a
Temple, K.
d63e7c66-9fb0-46c8-855d-ee2607e6c226
Mumford, A.D.
e874dcc4-7a3e-49a7-9c4c-461169f3bb39

Siddiq, S., Bower, K., Temple, K. and Mumford, A.D. (2004) Clinical and laboratory features of seven British kindreds with hereditary hyperferritinaemia cataract syndrome. British Journal of Haematology, 125 (s1), p.33. (doi:10.1111/j.1365-2141.2004.4894.x).

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More information

Published date: April 2004
Additional Information: Abstracts of the papers presented at the Annual Scientific Meeting of the British Society for Haematology Cardiff, UK 19-21 April 2004. No. 105.

Identifiers

Local EPrints ID: 60709
URI: http://eprints.soton.ac.uk/id/eprint/60709
ISSN: 0007-1048
PURE UUID: d1ee341b-c627-49ea-9863-04999171a0ad
ORCID for K. Temple: ORCID iD orcid.org/0000-0002-6045-1781

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Date deposited: 17 Nov 2008
Last modified: 16 Mar 2024 03:03

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Contributors

Author: S. Siddiq
Author: K. Bower
Author: K. Temple ORCID iD
Author: A.D. Mumford

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