(Q78234074)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

title

Restriction fragment analysis as a source of error in detection of heteroplasmic mtDNA mutations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

1 reference

S Finnilä

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

I E Hassinen

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

K Majamaa

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

language of work or name

English

0 references

publication date

1 August 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

volume

406

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

issue

2-4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

page(s)

109-114

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

Mitochondrial DNA sequence variation in human evolution and disease.

12 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Molecular genetic aspects of human mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Rapid detection of mitochondrial sequence polymorphisms using multiplex solid-phase fluorescent minisequencing

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Molecular scanning of candidate mitochondrial tRNA genes in type 2 (non-insulin dependent) diabetes mellitus.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritis

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Intracellular mitochondrial triplasmy in a patient with two heteroplasmic base changes

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Purification of mitochondrial DNA from human cell cultures and placenta

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

The human COL11A2 gene structure indicates that the gene has not evolved with the genes for the major fibrillar collagens

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Multiple independent occurrence of the 3243 mutation in mitochondrial tRNA(leuUUR) in patients with the MELAS phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5726%2899%2900007-2

7 January 2021

10.1016/S1383-5726(99)00007-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10479727%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

1 reference