Expanding the clinical phenotype of CAPN1-associated mutations: A new case with congenital-onset pure spastic paraplegia.

Authors :: Travaglini L
Bellacchio E
Aiello C
Pro S
Bertini E
Nicita F
Source :: Journal of the neurological sciences [J Neurol Sci] 2017 Jul 15; Vol. 378, pp. 210-212. Date of Electronic Publication: 2017 May 10.
Publication Year :: 2017

Subjects :: Adolescent
Calpain metabolism
Family
Humans
Male
Models, Molecular
Sequence Alignment
Spastic Paraplegia, Hereditary physiopathology
Spastin genetics
Calpain genetics
Mutation
Spastic Paraplegia, Hereditary genetics

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