A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2): HINTS FOR AN INTRACELLULAR FUNCTION AT THE SYNAPSE

Proline-rich transmembrane protein 2 (PRRT2) has been identified as the single causative gene for a group of paroxysmal syndromes of infancy, including epilepsy, paroxysmal movement disorders, and migraine. On the basis of topology predictions, PRRT2 has been assigned to the recently characterized f...

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Detalhes bibliográficos
Publicado no:J Biol Chem
Main Authors: Rossi, Pia, Sterlini, Bruno, Castroflorio, Enrico, Marte, Antonella, Onofri, Franco, Valtorta, Flavia, Maragliano, Luca, Corradi, Anna, Benfenati, Fabio
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2016
Assuntos:
Cell Biology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4813553/
https://ncbi.nlm.nih.gov/pubmed/26797119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M115.683888
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