Genetic Variation of CACNA1H in Idiopathic Generalized Epilepsy [1]

Annals of Neurology

Volumn 55, Issue 4, 2004, Pages 595-596

  Heron, Sarah E ^a   Phillips, Hilary A ^a   Mulley, John C ^a   Mazarib, Aziz ^b   Neufeld, Miriam Y ^b   Berkovic, Samuel F ^c   Scheffer, Ingrid E ^c,d  

^a WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^b TEL AVIV SOURASKY MEDICAL CENTER   (Israel)

^c UNIVERSITY OF MELBOURNE   (Australia)

^d ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL T TYPE;

ABSENCE; CACNA1H GENE; CONTROLLED STUDY; FEBRILE CONVULSION; FEMALE; GENE; GENE AMPLIFICATION; GENERALIZED EPILEPSY; GENETIC PREDISPOSITION; GENETIC VARIABILITY; HUMAN; IDIOPATHIC DISEASE; LETTER; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PRIORITY JOURNAL;

CALCIUM CHANNELS, T-TYPE; EPILEPSY, GENERALIZED; FEMALE; HUMANS; MALE; PEDIGREE; VARIATION (GENETICS);

EID: 1642372685     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20028     Document Type: Letter

References (3)

1. Chen Y, Lu J, Pan H, et al. Association between genetic variation of CACNA1H and childhood absence epilepsy. Ann Neurol 2003;54:239-243.
2. Gargus JJ. Unraveling monogenic channelopathies and their implications for complex polygenic disease. Am J Hum Genet 2003;72:785-803.
3. A-receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plus. Am J Hum Genet 2002;70:530-536.