(Q33681590)

28 July 2017

title

Pitfalls in the diagnosis of mtDNA mutations (English)

1 reference

28 July 2017

Seneca S

1

1 reference

28 July 2017

Lissens W

2

1 reference

28 July 2017

Liebaers I

3

1 reference

28 July 2017

van den Bergh P

4

1 reference

28 July 2017

Nassogne MC

5

1 reference

28 July 2017

Benatar A

6

1 reference

28 July 2017

de Meirleir L

7

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 November 1998

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

35

1 reference

28 July 2017

issue

11

1 reference

28 July 2017

page(s)

963-964

1 reference

A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathy.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051498

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051498

Compilation of tRNA sequences and sequences of tRNA genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051498

Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051498

Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051498

Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9832049

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9832049

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.35.11.963

1 reference

28 July 2017

1 reference

28 July 2017

1 reference