C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis.
about
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12Impairment of Drosophila orthologs of the human orphan protein C19orf12 induces bang sensitivity and neurodegenerationNeurodegeneration with brain iron accumulation: diagnosis and managementLate-onset neurodegeneration with brain iron accumulation with diffusion tensor magnetic resonance imagingNewly characterized forms of neurodegeneration with brain iron accumulation.C19orf12 mutation leads to a pallido-pyramidal syndrome.Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories.Excess iron harms the brain: the syndromes of neurodegeneration with brain iron accumulation (NBIA).Review: iron metabolism and the role of iron in neurodegenerative disorders.Iron and Neurodegeneration: Is Ferritinophagy the Link?Brain iron quantification by MRI in mitochondrial membrane protein-associated neurodegeneration under iron-chelating therapy.GeneHancer: genome-wide integration of enhancers and target genes in GeneCards.Rapid disease progression in adult-onset mitochondrial membrane protein-associated neurodegeneration.Iron regulatory protein (IRP)-iron responsive element (IRE) signaling pathway in human neurodegenerative diseases.Clinical and imaging characteristics of late onset mitochondrial membrane protein-associated neurodegeneration (MPAN)PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation.Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutation.ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree.Movement disorders in mitochondrial disease.
P2860
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P2860
C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis.
description
2012 nî lūn-bûn
@nan
2012 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
C19orf12 mutations in neurodeg ...... amyotrophic lateral sclerosis.
@ast
C19orf12 mutations in neurodeg ...... amyotrophic lateral sclerosis.
@en
type
label
C19orf12 mutations in neurodeg ...... amyotrophic lateral sclerosis.
@ast
C19orf12 mutations in neurodeg ...... amyotrophic lateral sclerosis.
@en
prefLabel
C19orf12 mutations in neurodeg ...... amyotrophic lateral sclerosis.
@ast
C19orf12 mutations in neurodeg ...... amyotrophic lateral sclerosis.
@en
P2093
P2860
P1433
P1476
C19orf12 mutations in neurodeg ...... amyotrophic lateral sclerosis.
@en
P2093
P2860
P2888
P304
P356
10.1007/S00415-012-6521-7
P577
2012-05-15T00:00:00Z
P5875
P6179
1025625551