Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.
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A. Hoischen | N. Drouot | J. Veltman | A. Durr | M. Koenig | A. Brice | G. Stevanin | C. Gilissen | B. Kremer | H. Lochmüller | H. Scheffer | Nienke Wieskamp | N. Knoers | S. Vermeer | P. Arts | K. Neveling | J. van der Wijst | C. Goizet | E. Kamsteeg | A. D. de Brouwer | M. Anheim | M. Kwint | A. David | R. Meijer | V. Milic-Rasic | M. Schijvenaars | Michael P. Kwint | A. Heister | M. Assoum | S. Todorovic | B. V. D. van de Warrenburg | V. Milić-Rašić
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