Novel mutations in the KCNJ10 gene associated to a...

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neurogenetics 2020 / 2

Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype

Morin, Matias, Forst, Anna-Lena, Pérez-Torre, Paula, Jiménez-Escrig, Adriano, Barca-Tierno, Verónica, García-Galloway, Eva, Warth, Richard, Lopez-Sendón Moreno, Jose Luis, Moreno-Pelayo, Miguel A
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Journal:
neurogenetics
DOI:
10.1007/s10048-020-00605-6
Date:
February, 2020
File:
PDF, 646 KB
2020
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