Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/46301
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Type: Journal article
Title: X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
Author: Dibbens, L.
Tarpey, P.
Hynes, K.
Bayly, M.
Scheffer, I.
Smith, R.
Bomar, J.
Sutton, E.
Vandeleur, L.
Shoubridge, C.
Edkins, S.
Turner, S.
Stevens, C.
O'Meara, S.
Tofts, C.
Barthorpe, S.
Buck, G.
Cole, J.
Halliday, K.
Jones, D.
et al.
Citation: Nature Genetics, 2008; 40(6):776-781
Publisher: Nature Publishing Group
Issue Date: 2008
ISSN: 1061-4036
1546-1718
Statement of
Responsibility: 
Leanne M Dibbens, Patrick S Tarpey, Kim Hynes, Marta A Bayly, Ingrid E Scheffer, Raffaella Smith, Jamee Bomar, Edwina Sutton, Lucianne Vandeleur, Cheryl Shoubridge, Sarah Edkins, Samantha J Turner, Claire Stevens, Sarah O'Meara, Calli Tofts, Syd Barthorpe, Gemma Buck, Jennifer Cole, Kelly Halliday, David Jones, Rebecca Lee, Mark Madison, Tatiana Mironenko, Jennifer Varian, Sofie West, Sara Widaa, Paul Wray, John Teague, Ed Dicks, Adam Butler, Andrew Menzies, Andrew Jenkinson, Rebecca Shepherd, James F Gusella, Zaid Afawi, Aziz Mazarib, Miriam Y Neufeld, Sara Kivity, Dorit Lev, Tally Lerman-Sagie, Amos D Korczyn, Christopher P Derry, Grant R Sutherland, Kathryn Friend, Marie Shaw, Mark Corbett, Hyung-Goo Kim, Daniel H Geschwind, Paul Thomas, Eric Haan, Stephen Ryan, Shane McKee, Samuel F Berkovic, P Andrew Futreal, Michael R Stratton, John C Mulley & Jozef Gécz
Abstract: Epilepsy and mental retardation limited to females (EFMR) is a disorder with an X-linked mode of inheritance and an unusual expression pattern. Disorders arising from mutations on the X chromosome are typically characterized by affected males and unaffected carrier females. In contrast, EFMR spares transmitting males and affects only carrier females. Aided by systematic resequencing of 737 X chromosome genes, we identified different protocadherin 19 (PCDH19) gene mutations in seven families with EFMR. Five mutations resulted in the introduction of a premature termination codon. Study of two of these demonstrated nonsense-mediated decay of PCDH19 mRNA. The two missense mutations were predicted to affect adhesiveness of PCDH19 through impaired calcium binding. PCDH19 is expressed in developing brains of human and mouse and is the first member of the cadherin superfamily to be directly implicated in epilepsy or mental retardation.
Keywords: Animals; Humans; Mice; Brain; Fibroblasts; Mental Retardation, X-Linked; Epilepsy; Cadherins; Case-Control Studies; Reverse Transcriptase Polymerase Chain Reaction; Pedigree; In Situ Hybridization; Cognition Disorders; Phenotype; Mutation, Missense; Gene Expression Regulation, Developmental; Genomic Imprinting; Chromosomes, Human, X; Genes, X-Linked; Codon, Nonsense; RNA, Messenger; Skin; Female; Male
Rights: Copyright © 2008 Nature Publishing Group
RMID: 0020080806
DOI: 10.1038/ng.149
Published version: http://www.nature.com/ng/journal/v40/n6/pdf/ng.149.pdf
Appears in Collections:Paediatrics publications

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