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contentType Journal Article|Research Support, Non-U.S. Gov't
endingPage 135
issn 1059-7794
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publicationName Human Mutation
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bibliographicCitation Salzmann A, Guipponi M, Lyons PJ, Fricker LD, Sapio M, Lambercy C, Buresi C, Ouled Amar Bencheikh B, Lahjouji F, Ouazzani R, Crespel A, Chaigne D, Malafosse A. Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy. Hum Mutat. 2012 Jan;33(1):124–35. doi: 10.1002/humu.21613. PMID: 21922598.
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date 2011-10-31^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1002/humu.21613
https://pubmed.ncbi.nlm.nih.gov/21922598
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language English
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https://pubmed.ncbi.nlm.nih.gov/
title Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy
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