(Q45746327)

15 December 2017

title

Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects (English)

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15 December 2017

author name string

Sha Tang

1

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15 December 2017

Jing Wang

2

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15 December 2017

Victor Wei Zhang

3

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15 December 2017

Fang-Yuan Li

4

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15 December 2017

Megan Landsverk

5

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15 December 2017

Hong Cui

6

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15 December 2017

Cavatina K Truong

7

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15 December 2017

Guoli Wang

8

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15 December 2017

Li Chieh Chen

9

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15 December 2017

Brett Graham

10

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15 December 2017

Fernando Scaglia

11

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15 December 2017

Eric S Schmitt

12

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15 December 2017

William J Craigen

13

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15 December 2017

Lee-Jun C Wong

14

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15 December 2017

publication date

2 April 2013

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15 December 2017

published in

Human Mutation

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15 December 2017

volume

34

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15 December 2017

issue

6

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15 December 2017

page(s)

882-893

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15 December 2017

What is a 'novel' mtDNA mutation--and does 'novelty' really matter?

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A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions

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Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Identifiers

DOI

10.1002/HUMU.22307

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15 December 2017

1 reference

15 December 2017