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Juvenile myoclonic epilepsy: disease expression among Indian families

โœ Scribed by S. Jain; M. V. Padma; A. Puri; M. C. Maheshwari

Book ID
109336732
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
794 KB
Volume
97
Category
Article
ISSN
0001-6314

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๐Ÿ“œ SIMILAR VOLUMES

Juvenile myoclonic epilepsy: An autosoma
Juvenile myoclonic epilepsy: An autosomal recessive disease
โœ Prof. Chrysostomos P. Panayiotopoulos; Tahir Obeid ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 399 KB

We undertook genetic study of patients with juvenile myoclonic epilepsy (JME) from 17 families. There was a mean of 8 children in each sibship. Siblings were affected in 8 sibships, and some families had more than 2 members affected by JME. Half-siblings and parental involvement were found in only 1

Juvenile myoclonic epilepsy: Linkage to
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โœ Bai, Dongsheng ;Alonso, Maria E. ;Medina, Marco T. ;Bailey, Julia N. ;Morita, Ry ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 134 KB

## Abstract Juvenile myoclonic epilepsy is a common subtype of idiopathic epilepsy accounting for 4โ€“11% of all epilepsies. We reported previously significant evidence of linkage between chromosome 6p12โ€“11 microsatellites and the clinical epilepsy and EEG traits of JME families from Belize and Los A