ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype - Concepedia

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ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype

27

Citations

20

References

2018

Year

Lorenzo Nanetti, Elisa Sarto, Anna Castaldo, Stefania Magri, Alessia Mongelli, Davide Rossi Sebastiano, Laura Canafoglia, Marina Grisoli, Chiara Malaguti, Francesca Rivieri,

Journal of Neurology

Mendelian DisorderGenetic DisorderGeneticsAno10 Mutational ScreeningClinical GeneticsRecessive AtaxiaNeurologyClinical PhenotypeDisease Gene IdentificationMedicineNeurogenetics

References

	Year	Citations

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