SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy
Titel:
SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy
Auteur:
Svenstrup, Kirsten Nielsen, Troels Tolstrup Aidt, Frederik Rostgaard, Nina Duno, Morten Wibrand, Flemming Vinther-Jensen, Tua Law, Ian Vissing, John Roos, Peter Hjermind, Lena Elisabeth Nielsen, Jørgen Erik