z-logo
Premium
Lafora progressive myoclonus epilepsy mutation database‐EPM2A and NHLRC1 (EMP2B) genes
Author(s) -
Ianzano Leonarda,
Zhang Junjun,
Chan Elayne M.,
Zhao XiaoChu,
Lohi Hannes,
Scherer Stephen W.,
Minassian Berge A.
Publication year - 2005
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.9376
Subject(s) - lafora disease , progressive myoclonus epilepsy , frameshift mutation , missense mutation , biology , genetics , myoclonus , nonsense mutation , epilepsy , gene , mutation , neuroscience , phosphatase , phosphorylation

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom