Varaico: Literature-Extracted Genetic Variants

Gene:FA2H
Variant:p.Y170*
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FA2H

NM_024306.5:p.Y170*

Associated Papers

A novel neurodegenerative spectrum disorder in patients with MLKL deficiency.

Faergeman SL et al.

Cell Death & Disease, 2020

FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.

Rattay TW et al.

Brain : a Journal of Neurology, 2019

Hereditary spastic paraplegia type 35 caused by a novel FA2H mutation.

Bektaş G et al.

The Turkish Journal of Pediatrics, 2017

Novel FA2H mutation in a girl with familial spastic paraplegia.

Aguirre-Rodríguez FJ et al.

Journal of the Neurological Sciences, 2015

Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis.

Zaki MS et al.

Clinical Genetics, 2015

Cerebral Iron Accumulation Is Not a Major Feature of FA2H/SPG35.

Marelli C et al.

Movement Disorders Clinical Practice, 2015

Phenotypic variability of a likely FA2H founder mutation in a family with complicated hereditary spastic paraplegia.

Donkervoort S et al.

Clinical Genetics, 2014

Heterozygous FA2H mutations in autism spectrum disorders.

Scheid I et al.

Bmc Medical Genetics, 2013

Novel Mutations in FA2H-Associated Neurodegeneration: An Underrecognized Condition?

Rupps R et al.

Journal of Child Neurology, 2013

A rare family with Hereditary Spastic Paraplegia Type 35 due to novel FA2H mutations: a case report with literature review.

Cao L et al.

Journal of the Neurological Sciences, 2013

Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation.

Tonelli A et al.

European Journal of Neurology, 2012

FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype.

Garone C et al.

Developmental Medicine and Child Neurology, 2011

Central nervous system dysfunction in a mouse model of FA2H deficiency.

Potter KA et al.

Glia, 2011

Genetics of neurodegeneration with brain iron accumulation.

Gregory A et al.

Current Neurology and Neuroscience Reports, 2011

Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA).

Kruer MC et al.

Annals of Neurology, 2010

Neurodegeneration with brain iron accumulation.

Gregory A et al.

Folia Neuropathologica, 2005

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."