Monozygotic twins with infantile neuroaxonal dystrophy: A case report and literature review - Wikidata - wikimedia - TriplyDB

Monozygotic twins with infantile neuroaxonal dystrophy: A case report and literature review

Monozygotic twins with infantile neuroaxonal dystrophy: A case report and literature review

http://www.wikidata.org/entity/Q31144455

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Monozygotic twins with infantile neuroaxonal dystrophy: A case report and literature review

http://www.wikidata.org/entity/Q31144455

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2016 nî lūn-bûn

@nan

2016 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

name

Monozygotic twins with infanti ...... e report and literature review

@ast

Monozygotic twins with infanti ...... e report and literature review

@en

type

label

Monozygotic twins with infanti ...... e report and literature review

@ast

Monozygotic twins with infanti ...... e report and literature review

@en

prefLabel

Monozygotic twins with infanti ...... e report and literature review

@ast

Monozygotic twins with infanti ...... e report and literature review

@en

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Experimental and Therapeutic Medicine

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Monozygotic twins with infanti ...... e report and literature review

@en

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Haifeng Li

http://www.w3.org/2001/XMLSchema#string

Hui Wang

http://www.w3.org/2001/XMLSchema#string

Huiying Jin

http://www.w3.org/2001/XMLSchema#string

Jiangping Wang

http://www.w3.org/2001/XMLSchema#string

Xiaoyan Tang

http://www.w3.org/2001/XMLSchema#string

Xinhua Bao

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Yan Zou

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Yuping Che

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P2860

Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN).

Infantile neuroaxonal dystrophy: what's most important for the diagnosis?

Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy.

PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron.

PLA2G6 mutation underlies infantile neuroaxonal dystrophy

Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6

Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations

Neurodegeneration associated with genetic defects in phospholipase A(2).

Extensive aggregation of α-synuclein and tau in juvenile-onset neuroaxonal dystrophy: an autopsied individual with a novel mutation in the PLA2G6 gene-splicing site

Mouse models of human INAD by Pla2g6 deficiency.

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3387-3389

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scholarly article

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10.3892/ETM.2016.3761

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5

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12

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2016-09-30T00:00:00Z

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27882168

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5103811

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