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Human Mutation
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May 25, 2012
PRRT2 mutations are the major cause of benign familial infantile seizures
Julian Schubert, Roberta Paravidino, Felicitas Becker, et al.
Nature Genetics
|
November 3, 2014
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
Julian Schubert, Aleksandra Siekierska, Mélanie Langlois, et al.
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of 9
Search research articles
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Showing results (81-90 of 82) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 82 results.
Human Mutation
|
May 25, 2012
PRRT2 mutations are the major cause of benign familial infantile seizures
Julian Schubert, Roberta Paravidino, Felicitas Becker, et al.
Nature Genetics
|
November 3, 2014
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
Julian Schubert, Aleksandra Siekierska, Mélanie Langlois, et al.
Page
of 9