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Sporadic Infantile Epileptic Encephalopathy Caused by Mut... | ResearchHub
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Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
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Authors
Christel Depienne
•
Delphine Bouteiller
22 more
•
Eric Leguern
Published
February 13, 2009
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Journal
PLoS Genetics
Topics
Neuroscience
Biology
Neuroscience
Genetics
Missense Mutation
Rett Syndrome
Show all topics
DOI
10.1371/journal.pgen.1000381
License
CC-BY
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