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Atypical Adult Onset Complicated Spastic Paraparesis with Thin Corpus Callosum in Two Patients Carrying a Novel FA2H Mutation

Overview
Journal Eur J Neurol
Publisher Wiley
Specialty Neurology
Date 2012 Aug 29
PMID 22925154
Citations 11
Authors
A Tonelli
M G DAngelo
F Arrigoni
E Brighina
A Arnoldi
A Citterio
N Bresolin
M T Bassi
Affiliations
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FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.

Rattay T, Lindig T, Baets J, Smets K, Deconinck T, Sohn A Brain. 2019; 142(6):1561-1572.

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Cerebral Iron Accumulation Is Not a Major Feature of /SPG35.

Marelli C, Salih M, Nguyen K, Mallaret M, Leboucq N, Hassan H Mov Disord Clin Pract. 2019; 2(1):56-60.

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Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features.

Incecik F, Besen S, Bozdogan S Ann Indian Acad Neurol. 2018; 21(4):335-339.

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Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature review.

Mari F, Berti B, Romano A, Baldacci J, Rizzi R, Grazia Alessandri M Neurogenetics. 2018; 19(2):123-130.

PMID: 29423566 DOI: 10.1007/s10048-018-0538-8.