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HARVARD Citation
Mendoza-Ferreira, N. et al. (2018). Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function. Neurology. p. . [Online].
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Mendoza-Ferreira, N. et al. (2018). Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function. Neurology. p. . [Online].