Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations.
Uirá Souto MeloF FreuaD S LynchB D RipaR B TenorioJonas Alex Morales SauteF de Souza LeiteJ KitajimaH HouldenM ZatzFernando KokPublished in: Clinical genetics (2018)
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