Disease: Myoclonic epilepsy of infancy

Human Genetics

Volumn 127, Issue 4, 2010, Pages 463-

  Rocca, F E ^a   De Marco, E V ^a   Annesi, F ^a   Civitelli, D ^a   Provenzano, G ^a   Sproviero, W ^a   Scornaienchi, V ^a   Greco, V ^a   Tarantino, P ^a   Annesi, G ^a  

^a Cosenza ISN CNR ^*  (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHANNEL NAV1.1; NERVE PROTEIN; SODIUM CHANNEL; SODIUM CHANNEL, VOLTAGE GATED, TYPE I, ALPHA PROTEIN; SODIUM CHANNEL, VOLTAGE-GATED, TYPE I, ALPHA PROTEIN;

INFANT DISEASE; MYOCLONUS EPILEPSY; NOTE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; AMINO ACID SUBSTITUTION; ARTICLE; CODON; GENETICS; HUMAN; INFANT; STOP CODON;

AMINO ACID SUBSTITUTION; BASE SEQUENCE; CODON; CODON, NONSENSE; EPILEPSIES, MYOCLONIC; HUMANS; INFANT; NERVE TISSUE PROTEINS; SODIUM CHANNELS;

EID: 84863681976     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-010-0788-5     Document Type: Note

References (0)