(Q41375604)

30 September 2017

1 reference

title

Bottlenecks and beyond: mitochondrial DNA segregation in health and disease (English)

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30 September 2017

0 references

Brown GK

1

1 reference

30 September 2017

1 March 1997

1 reference

Journal of Inherited Metabolic Disease

30 September 2017

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30 September 2017

20

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30 September 2017

1

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30 September 2017

2-8

1 reference

https://scigraph.springernature.com/pub.10.1023/a:1005336903888

30 September 2017

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cites work

Rapid segregation of heteroplasmic bovine mitochondria

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissues.

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

Mitochondrial gene segregation in mammals: is the bottleneck always narrow?

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

Molecular genetic characterization of an X-linked form of Leigh's syndrome.

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

Intracellular heteroplasmy for disease-associated point mutations in mtDNA: implications for disease expression and evidence for mitotic segregation of heteroplasmic units of mtDNA.

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

Mitochondrial DNA copy number in bovine oocytes and somatic cells

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

Leigh syndrome resulting from de novo mutation at position 8993 of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1005336903888

7 January 2021

Identifiers

DOI

10.1023/A:1005336903888

1 reference

PubMed ID

9061561

Dimensions Publication ID

30 September 2017

0 references

1 reference

PubMed ID

9061561