Supporting evidence of a gene for partial epilepsy on 10q

Neurogenetics

Volumn 3, Issue 1, 2000, Pages 31-34

  Mautner, Victor F ^a   Lindenau, Matthias ^a   Gottesleben, Arnd ^a   Goetze, Gisela ^a   Kluwe, Lan ^b  

^a Klinik Ochsenzoll   (Germany)

^b UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

Author keywords

10q; Epilepsy; Partial seizure

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 10; CHROMOSOME MAP; ELECTROENCEPHALOGRAPHY; FEMALE; GENETIC LINKAGE; GENETIC MARKER; GENETIC RECOMBINATION; GENETICS; HUMAN; MALE; PATHOPHYSIOLOGY; PEDIGREE; PHENOTYPE; TEMPORAL LOBE EPILEPSY;

ADULT; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; ELECTROENCEPHALOGRAPHY; EPILEPSY, TEMPORAL LOBE; FEMALE; GENETIC MARKERS; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; PEDIGREE; PHENOTYPE; RECOMBINATION, GENETIC;

EID: 85047680420     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100480000091     Document Type: Article

References (16)

1. Beck-Mannagetta G, Janz D (1992) Genetik und genetische Beratung. In: Hopf HC, Poeck K, Schliack H (eds) Neurologie in Praxis und Klinik, Band 1. Thieme, Stuttgart, 3.57-3.63
2. Ottman R (1989) Genetics of the partial epilepsies: a review. Epilepsia 30:107-111
3. Ottman R, Annegers JF, Hauser WA, Kurland WT (1989) Seizure risk in offspring of parents with generalized versus partial epilepsy. Epilepsia 30: 157-161
4. Treimann DM (1989) Genetics of the partial epilepsies. In: Beck-Mannagetta G, Anderson VE, Doose H, Janz D (eds) Genetics of the epilepsies. Springer, Berlin Heidelberg, New York, pp 73-82
5. Degen R, Degen HE, Konecke B (1993) On the genetics of complex partial seizures: walking and sleep EEGs in siblings. J Neurol 240:151-155
6. Steinlein OK, Mulley JC, Propping P, Wallace RH, Phillips HA, Sutherland GR, Scheffer IE, Berkovic SF (1995) A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal epilepsy. Nat Genet 11:201-203
7. Steinlein OK, Magnusson A, Stoodt J, Bertrand S, Weiland S, Berkovic SF, Nakken KO, Propping P, Bertrand D (1997) An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy. Hum Mol Genet 6:943-947
8. Abou-Khalil B, Andermann E, Andermann F, Olivier A, Quesney LF (1993) Temporal lobe epilepsy after prolonged febrile convulsions: excellent outcome after surgical treatment. Epilepsia 34:878-883
9. Berkovic SF, McIntosh A, Howell RA, Mitchell A, Sheffield LJ, Hopper JL (1996) Familial temporal lobe epilepsy: a common disorder identified in twins. Ann Neurol 40:227-235
10. Ottman R, Risch N, Hauser WA, et al (1995) Localization of a gene for epilepsy to chromosome 10q. Nat Genet 10:56-60
11. Poza JJ, Sáenz A, Martinnez-Gil A, et al (1999) Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. Ann Neurol 45:182-188
12. American Electroencephalographic Society (1991) Guidelines for standard electrode position nomenclature. J Clin Neurophysiol 8:200-222
13. American Electroencephalographic Society (1986) Guidelines in EEG, 1-7. J Clin Neurophysiol 3:131-168
14. Commission on Classification and Terminology of the International League Against Epilepsy (1989) Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 30:389-399
15. Jackson GD, Berkovic SF, Duncan JS, Connelly A (1993) Optimizing the diagnosis of hippocampal sclerosis using MR imaging. AJNR 14:753-762
16. Lathrop CM, Lalouel JM, Julier C, Ott J (1984) Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci U S A 81:3443-3446