Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): Confirmation of linkage to human chromosome 16p12-q12 in a Chinese family
10.1007/s004390050876
Saved in:
Main Authors: | Lee, W.-L., Tay, A., Ong, H.-T., Goh, L.-M., Monaco, A.P., Szepetowski, P. |
---|---|
Other Authors: | INSTITUTE OF MOLECULAR & CELL BIOLOGY |
Format: | Article |
Published: |
2014
|
Online Access: | http://scholarbank.nus.edu.sg/handle/10635/116233 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
Similar Items
-
Transient paroxysmal dyskinesia associated with focal basal ganglia lesions
by: See S.-J., et al.
Published: (2018) -
PRRT2 Gene Analysis of Paroxysmal Kinesigenic Dyskinesia (PKD) in Thai Children
by: Laosuebsakulthai P.
Published: (2023) -
Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations
by: Tan L.C.S., et al.
Published: (2018) -
PRRT2 Gene Analysis of Paroxysmal Kinesigenic Dyskinesia (PKD) in Thai Children
by: Pantaree Laosuebsakulthai, et al.
Published: (2022) -
Genetic susceptibility to asthma and atopy among Chinese in Singapore - Linkage to markers on chromosome 5q31-33
by: Shek, L.P.-C., et al.
Published: (2013)