Johnnys Kcnma1 Story - Right I need the power of FB to work some good here. I am turning my feeling of being useless to help Johnny into something positive and I
![BK channel properties correlate with neurobehavioral severity in three KCNMA1-linked channelopathy mouse models | bioRxiv BK channel properties correlate with neurobehavioral severity in three KCNMA1-linked channelopathy mouse models | bioRxiv](https://www.biorxiv.org/content/biorxiv/early/2022/02/16/2022.02.15.478992.1/F1.large.jpg)
BK channel properties correlate with neurobehavioral severity in three KCNMA1-linked channelopathy mouse models | bioRxiv
![Cancers | Free Full-Text | KCNMA1 Expression Is Downregulated in Colorectal Cancer via Epigenetic Mechanisms Cancers | Free Full-Text | KCNMA1 Expression Is Downregulated in Colorectal Cancer via Epigenetic Mechanisms](https://www.mdpi.com/cancers/cancers-11-00245/article_deploy/html/images/cancers-11-00245-g008.png)
Cancers | Free Full-Text | KCNMA1 Expression Is Downregulated in Colorectal Cancer via Epigenetic Mechanisms
![Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia | PNAS Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia | PNAS](https://www.pnas.org/cms/10.1073/pnas.1920008117/asset/b6845bce-e1f1-417d-8149-096f5885ff0e/assets/graphic/pnas.1920008117fig02.jpeg)
Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia | PNAS
![Frontiers | Molecular Mechanisms of Epileptic Encephalopathy Caused by KCNMA1 Loss-of-Function Mutations Frontiers | Molecular Mechanisms of Epileptic Encephalopathy Caused by KCNMA1 Loss-of-Function Mutations](https://www.frontiersin.org/files/Articles/775328/fphar-12-775328-HTML/image_m/fphar-12-775328-g001.jpg)
Frontiers | Molecular Mechanisms of Epileptic Encephalopathy Caused by KCNMA1 Loss-of-Function Mutations
![KCNMA1 mutation in children with paroxysmal dyskinesia and epilepsy: Case report and literature review - IOS Press KCNMA1 mutation in children with paroxysmal dyskinesia and epilepsy: Case report and literature review - IOS Press](https://content.iospress.com/media/trd/2017/2-3-4/trd-2-3-4-trd018/trd-2-trd018-g001.jpg?width=755)
KCNMA1 mutation in children with paroxysmal dyskinesia and epilepsy: Case report and literature review - IOS Press
![KCNMA1 mutation in children with paroxysmal dyskinesia and epilepsy: Case report and literature review - IOS Press KCNMA1 mutation in children with paroxysmal dyskinesia and epilepsy: Case report and literature review - IOS Press](https://content.iospress.com/media/trd/2017/2-3-4/trd-2-3-4-trd018/trd-2-trd018-g002.jpg?width=755)
KCNMA1 mutation in children with paroxysmal dyskinesia and epilepsy: Case report and literature review - IOS Press
![KCNMA1 gene expression in five molecular subtypes of breast cancer.... | Download Scientific Diagram KCNMA1 gene expression in five molecular subtypes of breast cancer.... | Download Scientific Diagram](https://www.researchgate.net/profile/Han-Gang-Yu/publication/342479259/figure/fig1/AS:1146039646064640@1650248552009/KCNMA1-gene-expression-in-five-molecular-subtypes-of-breast-cancer-Each-dot-represents.png)
KCNMA1 gene expression in five molecular subtypes of breast cancer.... | Download Scientific Diagram
![MitoBK(Ca) is encoded by the Kcnma1 gene, and a splicing sequence defines its mitochondrial location. - Abstract - Europe PMC MitoBK(Ca) is encoded by the Kcnma1 gene, and a splicing sequence defines its mitochondrial location. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3696804/bin/pnas.1302028110fig07.jpg)