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(PDF) Neuropathology of SCA34 showing widespread oligodendroglial ...
Light microscopic features of SCA34 in cerebellum. a–b... | Download ...
SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage ...
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L168F SCA34 mutant suppresses very long chain saturated FA synthesis ...
Combined multipoint LOD score analyses of the SCA34 locus. A) The ...
Additional European families map to the SCA34 locus. The disease ...
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Results of the cognitive evaluation in patients with SCA34 and controls ...
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Characterization of the phenotype with cognitive impairment and protein ...
Gross physical phenotype of SCA34-KI rats. a Gross appearance of WT and ...
Gross and semi-macroscopic features of SCA34. a, b Inferior views of ...
Light microscopic observation of white matter vacuoles in an autopsy ...
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Microscopic observation of the pons and cerebellum from an autopsy case ...
Tauopathy in SCA34. a and b The subthalamic nucleus showing frequent ...
Compared features of ELOVL5/p.G230V/SCA38 and ELOVL4/p.W246G/SCA34 ...
Synapse-Specific Defects in Synaptic Transmission in the Cerebellum of ...
Macroscopic views of the brain of an autopsy case with SCA34. (a and b ...
Cone cells are preserved in the SCA34-KI rat retina. a–c Labeling of ...
Müller cells in the SCA34-KI rat retina are not reactive. a–c Müller ...
W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and ...
Frontiers | Neurocognition, cerebellar functions and psychiatric ...
(PDF) Characterization of the phenotype with cognitive impairment and ...
Cone cells are preserved in the SCA34-KI rat retina. a-c Labeling of ...
(PDF) W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and ...
(PDF) Novel ELOVL4 mutation associated with erythrokeratodermia and ...
ELOVL4 disease-causing variants and their frequency in the reported ...
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ELOVL4 Mutations That Cause Spinocerebellar Ataxia-34 Differentially ...
| Schematic representation of cerebellar afferents and efferents. (A ...
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Progressive symmetric erythrokeratodermia with spinocerebellar ataxia ...
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A (Left) Visualisation of full structure of human ELOVL4 protein using ...
Specific Biomarkers in Spinocerebellar Ataxia Type 3: A Systematic ...
(PDF) The Spinocerebellar Ataxia 34-Causing W246G ELOVL4 Mutation Does ...
Images Supporting the Clinical Diagnosis of Spinocerebellar Ataxia With ...
Very long chain fatty acid-containing lipids: a decade of novel ...
Sca-1 and CD34 expression is altered following acute bladder outlet ...
L168S ELOVL4 localizes properly to the Endoplasmic Reticulum (ER) but ...
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Incomplete Elongation of Ultra-long-chain Polyunsaturated Acyl-CoAs by ...
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(PDF) A family study and literature review of ELOVL4-associated ...
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Confirmation of the NM_022726.3: c.503 T > C de novo variant with ...
Clinical findings according to variant in reported cases of ATX-ELOVL4 ...
Distribution of VGluT2 and mGluR1 in WT, HET, and MUT rat cerebellum ...
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