(Q41730723)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

title

Variable genotype of Leber's hereditary optic neuropathy patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

hereditary optic neuropathy

27 September 2019

main subject

1 reference

M T Lott

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

A S Voljavec

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

D C Wallace

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

language of work or name

English

0 references

publication date

1 June 1990

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Ophthalmology

27 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

volume

109

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

page(s)

625-631

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

New aspects of the genetic, etiologic, and clinical puzzle of Leber's disease

27 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Maternal inheritance of human mitochondrial DNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Maternal inheritance of mitochondrial DNA polymorphisms in cultured human fibroblasts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Mitochondrial DNA in anucleate human blood cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Mitotic segregation of mitochondrial DNAs in human cell hybrids and expression of chloramphenicol resistance.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Mitochondria and Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Unequal partitioning of bovine mitochondrial genotypes among siblings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972429-8

10.1016/S0002-9394(14)72429-8

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346190%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

1 reference