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Type: Journal article
Title: Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations
Author: Corbett, M.
Turner, S.
Gardner, A.
Silver, J.
Stankovich, J.
Leventer, R.
Derry, C.
Carroll, R.
Ha, T.
Scheffer, I.
Bahlo, M.
Jackson, G.
Mackey, D.
Berkovic, S.
Gecz, J.
Citation: European Journal of Medical Genetics, 2017; 60(8):437-443
Publisher: Elsevier Masson SAS
Issue Date: 2017
ISSN: 1769-7212
Statement of
Mark A. Corbett, Samantha J. Turner, Alison Gardner, Jeremy Silver, Jim Stankovich, Richard J. Leventer, Christopher P. Derry Renée Carroll, Thuong Ha, Ingrid E. Scheffer, Melanie Bahlo, Graeme D. Jackson, David A. Mackey, Samuel F. Berkovic, Jozef Gecz
Abstract: Abstract not available
Keywords: COL18A1
Exome sequencing
Knobloch syndrome
Description: Available online 8 June 2017
Rights: Crown Copyright © 2017 Published by Elsevier Masson SAS. All rights reserved.
DOI: 10.1016/j.ejmg.2017.06.002
Grant ID:
Appears in Collections:Aurora harvest 8
Genetics publications

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