دورية أكاديمية
Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype
| العنوان: | Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype |
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| المؤلفون: | Morin, Matias, Forst, Anna-Lena, Pérez-Torre, Paula, Jiménez-Escrig, Adriano, Barca-Tierno, Verónica, García-Galloway, Eva, Warth, Richard, Lopez-Sendón Moreno, Jose LuisAff3, Moreno-Pelayo, Miguel AngelAff1 |
| المصدر: | neurogenetics. 21(2):135-143 |
| قاعدة البيانات: | Springer Nature Journals |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 13646745 13646753 |
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| DOI: | 10.1007/s10048-020-00605-6 |