(Q38714575)

5 September 2017

The clinical and genetic characteristics in children with mitochondrial disease in China (English)

1 reference

Erratum to: The clinical and genetic characteristics in children with mitochondrial disease in China

5 September 2017

mitochondrial disease

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based on heuristic

inferred from title

corrigendum / erratum

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author name string

Fang Fang

1

1 reference

5 September 2017

Zhimei Liu

2

1 reference

5 September 2017

Hezhi Fang

3

1 reference

5 September 2017

Jian Wu

4

1 reference

5 September 2017

Danmin Shen

5

1 reference

5 September 2017

Suzhen Sun

6

1 reference

5 September 2017

Changhong Ding

7

1 reference

5 September 2017

Tongli Han

8

1 reference

5 September 2017

Yun Wu

9

1 reference

5 September 2017

Junlan Lv

10

1 reference

5 September 2017

Lei Yang

11

1 reference

5 September 2017

Shufang Li

12

1 reference

5 September 2017

Jianxin Lv

13

1 reference

5 September 2017

Ying Shen

14

1 reference

5 September 2017

16 June 2017

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Science in China. Series C: Life Sciences

5 September 2017

1 reference

5 September 2017

60

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5 September 2017

7

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5 September 2017

746-757

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https://scigraph.springernature.com/pub.10.1007/s11427-017-9080-y

5 September 2017

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cites work

Multiple sclerosis and mitochondrial gene variations: a review

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Mitochondrial complex I deficiency: from organelle dysfunction to clinical disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Central nervous system manifestations of mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Leber's hereditary optic neuropathy mutations associated with infantile-onset myoclonic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Targeted exome sequencing of suspected mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Next-generation genetic testing for retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

A mitochondrial protein compendium elucidates complex I disease biology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Leigh syndrome: clinical features and biochemical and DNA abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

High-quality DNA sequence capture of 524 disease candidate genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

New SUCLG1 patients expanding the phenotypic spectrum of this rare cause of mild methylmalonic aciduria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

Next generation sequence analysis for mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

MELAS: a nationwide prospective cohort study of 96 patients in Japan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11427-017-9080-Y

10.1007/S11427-017-9080-Y

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

5 September 2017

1086109408

0 references

Fatcat ID

release_n2yt6566ojgltnlnbmwtwl5wpa

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/n2yt6566ojgltnlnbmwtwl5wpa

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference