Genes and epilepsy.
作者信息
Gardiner R M
机构信息
Department of Paediatrics, John Radcliffe Hospital, Headington, Oxford.
出版信息
J Med Genet. 1990 Sep;27(9):537-44. doi: 10.1136/jmg.27.9.537.
Abstract
摘要
相似文献
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Genes and epilepsy.基因与癫痫
J Med Genet. 1990 Sep;27(9):537-44. doi: 10.1136/jmg.27.9.537.
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引用本文的文献
1
Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p.8号染色体短臂上进行性癫痫伴智力障碍（EPMR）基因座的遗传和物理图谱分析。
Genome Res. 1996 May;6(5):351-60. doi: 10.1101/gr.6.5.351.
2
Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.家族性热性惊厥的一个主要基因定位于8q13 - 21的研究提示。
J Med Genet. 1996 Apr;33(4):308-12. doi: 10.1136/jmg.33.4.308.
3
Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q.良性家族性新生儿惊厥的遗传异质性：8号染色体长臂上新基因座的鉴定
Am J Hum Genet. 1993 Sep;53(3):670-5.
4
The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.一种与智力迟钝相关的隐性遗传人类儿童进行性癫痫的基因定位于8号染色体短臂远端。
Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7267-70. doi: 10.1073/pnas.91.15.7267.
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Genetic analysis of kifafa, a complex familial seizure disorder.基法法（一种复杂的家族性癫痫疾病）的基因分析
Am J Hum Genet. 1995 Oct;57(4):902-10.
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Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.进行性肌阵挛癫痫基因定位于21号染色体q22区。
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Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.良性家族性新生儿惊厥与D20S19和D20S20连锁关系的确认。
Hum Genet. 1992 Apr;89(1):54-8. doi: 10.1007/BF00207042.
本文引用的文献
1
HEREDITARY CHARACTERISTICS OF FAMILIAL TEMPORAL-CENTRAL FOCAL EPILEPSY.家族性颞中央局灶性癫痫的遗传特征
Pediatrics. 1965 Aug;36:207-11.
2
Hereditary aspects of epilepsy.
Bull Johns Hopkins Hosp. 1959 Nov;105:245-71.
3
Genetics of convulsive disorders. II. Genetic and electroencephalographic studies in centrencephalic epilepsy.惊厥性疾病的遗传学。II. 中央脑性癫痫的遗传学与脑电图研究。
Neurology. 1961 Jun;11:474-83. doi: 10.1212/wnl.11.6.474.
4
Genetic aspects of epilepsy.癫痫的遗传学方面
Folia Psychiatr Neurol Jpn. 1980;34(3):215-25. doi: 10.1111/j.1440-1819.1980.tb01530.x.
5
Juvenile myoclonic epilepsy of Janz.
Neurology. 1984 Mar;34(3):285-94. doi: 10.1212/wnl.34.3.285.
6
Role of the gamma-aminobutyric acid receptor-ionophore complex in seizure disorders.γ-氨基丁酸受体-离子载体复合物在癫痫疾病中的作用。
Ann Neurol. 1984;16 Suppl:S90-7. doi: 10.1002/ana.410160714.
7
Looking for epilepsy genes.寻找癫痫基因。
Ann Neurol. 1984;16 Suppl:S12-7. doi: 10.1002/ana.410160704.
8
Febrile convulsions in families: findings in an epidemiologic survey.
Clin Pediatr (Phila). 1966 Oct;5(10):604-8. doi: 10.1177/000992286600501007.
9
On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type. A clinical and electroencephalographic study of 399 probands.
Humangenetik. 1973 Jul 20;19(2):155-82. doi: 10.1007/BF00282192.
10
Genetic factors in spike-wave absences.
Epilepsia. 1973 Mar;14(1):57-75. doi: 10.1111/j.1528-1157.1973.tb03942.x.
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