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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

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Goncu, BEYZA


Ozgul, C.

Hasanoglu, S.

Yesil, G.

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2020-12-01T00:00:00Z

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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

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

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