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An unusual familial oculopharyngeal syndrome2

An unusual familial oculopharyngeal syndrome2
An unusual familial oculopharyngeal syndrome2
letter, genetics, italy, report, syndrome, muscular dystrophies, pharyngeal muscles, female, humans, adult, oculomotor muscles, pathology
1351-5101
549-550
Cooper, S. A.
350814ff-a48c-4f9d-92d7-22acf2df7dbf
Hill, M. E.
539ebddb-124c-41bc-995f-6d873e838671
Weller, R. O.
ae32be34-f49f-4944-bf93-19d54f3baac6
Hammans, S. R.
6553eac5-9322-4f2b-b677-d4ba698fc10b
Cooper, S. A.
350814ff-a48c-4f9d-92d7-22acf2df7dbf
Hill, M. E.
539ebddb-124c-41bc-995f-6d873e838671
Weller, R. O.
ae32be34-f49f-4944-bf93-19d54f3baac6
Hammans, S. R.
6553eac5-9322-4f2b-b677-d4ba698fc10b

Cooper, S. A., Hill, M. E., Weller, R. O. and Hammans, S. R. (2006) An unusual familial oculopharyngeal syndrome2. European Journal of Neurology, 13 (5), 549-550. (doi:10.1111/j.1468-1331.2006.01225.x).

Record type: Letter

Full text not available from this repository.

More information

Published date: May 2006
Keywords: letter, genetics, italy, report, syndrome, muscular dystrophies, pharyngeal muscles, female, humans, adult, oculomotor muscles, pathology

Identifiers

Local EPrints ID: 59605
URI: http://eprints.soton.ac.uk/id/eprint/59605
ISSN: 1351-5101
PURE UUID: 58d3a440-c6b0-45fb-9e36-5115c80edca1

Catalogue record

Date deposited: 04 Sep 2008
Last modified: 13 Mar 2019 20:30

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