☆ 4.5 Letter

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

JOURNAL OF THE NEUROLOGICAL SCIENCES (2017)

Journal

JOURNAL OF THE NEUROLOGICAL SCIENCES

Volume 378, Issue -, Pages 210-212

Publisher

ELSEVIER SCIENCE BV

DOI: 10.1016/j.jns.2017.05.014

Keywords

Hereditary spastic paraplegia; Central nervous system; CAPN1; Targeted resequencing; Ataxia; Calpains

Categories

Clinical Neurology Neurosciences

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