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Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.
Renaud, M., Tranchant, C., Martin, J. V. T., Mochel, F., et al. (2017). A recessive ataxia diagnosis algorithm for the next generation sequencing era. Annals of Neurology, 82(6), 892 - 899.
Barateiro, A., Chen, S., Yueh, M. - F., Fernandes, A., et al. (2016). Reduced myelination and increased glia reactivity resulting from severe neonatal hyperbilirubinemia. Molecular Pharmacology, 89(1), 84 - 93.
McGovern, M. M., Elles, R., Beretta, I., Somerville, M. J., et al. (2007). Report of an international survey of molecular genetic testing laboratories. Community Genetics, 10(3), 123 - 131.
Bettencourt, C., Quintáns, B., Ros, R., Ampuero, I., et al. (2012). Revisiting genotype-phenotype overlap in neurogenetics: Triplet-repeat expansions mimicking spastic paraplegias. Human Mutation, 33(9), 1315 - 1323.
Bettencourt, C., Quintáns, B., Ros, R., Ampuero, I., et al. (2012). Revisiting genotype-phenotype overlap in neurogenetics: Triplet-repeat expansions mimicking spastic paraplegias. Human Mutation, 33(9), 1315 - 1323.

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