Publication:
Identification and functional characterization of a novel homozygous mutation in KCNMA1 encoding voltage and calcium sensitive potassium channel is associated with dyskinesia, epilepsy, intellectual disability, cerebellar and corticospinal tract atrophy

Placeholder

Organizational Units

Program

Authors

Authors

Goncu, BEYZA
Aslanger, A.
Ozgul, C.
Hasanoglu, S.
Yesil, G.

Advisor

Date

2020-12-01T00:00:00Z

Language

Type

Article

Publisher

Journal Title

Journal ISSN

Volume Title

Abstract

Description

Source:

Keywords:

Keywords

Citation

YÜCESAN E., Goncu B., Aslanger A., Ozgul C., Hasanoglu S., Yesil G., -Identification and functional characterization of a novel homozygous mutation in KCNMA1 encoding voltage and calcium sensitive potassium channel is associated with dyskinesia, epilepsy, intellectual disability, cerebellar and corticospinal tract atrophy-, EUROPEAN JOURNAL OF HUMAN GENETICS, cilt.28, ss.344-345, 2020

URI

http://hdl.handle.net/20.500.12645/28367

Collections

Yayınlar - Eserler

Endorsement

Review

Supplemented By

Referenced By

0

Views

0

Downloads


Sustainable Development Goals