Résultats de la recherche

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(1 - 10 of 10)
A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia
Exonic deletions of FXN and early-onset Friedreich ataxia
Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy

Islandora displays