Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

Lancet

Volumn 358, Issue 9284, 2001, Pages 801-807

  Jouvenceau, Anne ^a,b   Eunson, Louise H ^a   Spauschus, Alexander ^a,c   Ramesh, Venkataswaran ^d   Zuberi, Sameer M ^e   Kullmann, Dimitri M ^a   Hanna, Michael G ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b INSERM   (France)

^c UNIVERSITY OF BONN   (Germany)

^d NEWCASTLE GENERAL HOSPITAL   (United Kingdom)

^e ROYAL HOSPITAL FOR SICK CHILDREN   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; COMPLEMENTARY DNA;

ARTICLE; ATAXIA; CARBOXY TERMINAL SEQUENCE; CHILD; ELECTROPHYSIOLOGY; GENE EXPRESSION; GENE MUTATION; GENE SEQUENCE; GENERALIZED EPILEPSY; GENETIC CODE; HUMAN; LEARNING DISORDER; MALE; POINT MUTATION; PRIORITY JOURNAL; STOP CODON;

EID: 0035828406     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(01)05971-2     Document Type: Article

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