Case report: A Chinese child with Andersen–Tawil syndrome due to a de novo KCNJ2 mutation.

Subjects

Subjects :

*CHINESE people
*GENETIC mutation
*NEUROLOGY
*PARALYSIS
*MEDICAL research
*DISEASES

Details

Language :

English

ISSN :

0022510X

Volume :

352

Issue :

1/2

Database :

Academic Search Index

Journal :

Journal of the Neurological Sciences

Publication Type :

Academic Journal

Accession number :

102217729

Full Text :

https://doi.org/10.1016/j.jns.2015.02.027