Novel variant in Moroccan patient with hereditary spastic paraplegia type 35
Author:
Funder
Campus France
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference20 articles.
1. Clinical and genetic investigations of three Moroccan families with retinitis Pigmentosa phenotypes;Bouzidi;Mol. Vis.,2021
2. A rare family with hereditary spastic paraplegia type 35 due to novel FA2H mutations: a case report with literature review;Cao;J. Neurol. Sci.,2013
3. Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35);Dick;Hum. Mutat.,2010
4. Mutations in the fatty acid 2-hydroxylase gene are associated with Leukodystrophy with spastic Paraparesis and dystonia;Edvardson;Am. J. Hum. Genet.,2008
5. Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance;Finsterer;J. Neurol. Sci.,2012
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