(Q33680431)

28 July 2017

Pancreatic exocrine dysfunction associated with mitochondrial tRNA(Leu)(UUR) mutation (English)

1 reference

28 July 2017

Onishi H

1

1 reference

28 July 2017

Hanihara T

2

1 reference

28 July 2017

Sugiyama N

3

1 reference

28 July 2017

Kawanishi C

4

1 reference

28 July 2017

Iseki E

5

1 reference

28 July 2017

Maruyama Y

6

1 reference

28 July 2017

Yamada Y

7

1 reference

28 July 2017

Kosaka K

8

1 reference

28 July 2017

Yagishita S

9

1 reference

28 July 2017

Sekihara H

10

1 reference

28 July 2017

Satoh S

11

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 March 1998

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

35

1 reference

28 July 2017

3

1 reference

28 July 2017

255-257

1 reference

Depressive disorder due to mitochondrial transfer RNALeu(UUR) mutation.

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

Maternally inherited diabetes and deafness: a new diabetes subtype

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

Mitochondrial DNA deletion in Pearson's marrow/pancreas syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

Diagnosis of pancreatic disease by a synthetic peptide. A new test of exocrine pancreatic function

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

Clinical spectrum of the MELAS mutation in a large pedigree.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and diabetes mellitus: molecular genetic analysis and family study.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

Mitochondrial myopathy and cardiomyopathy with neurodegenerative features and multiple brain infarcts.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051255

Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9541116

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.35.3.255

1 reference

28 July 2017

1 reference

28 July 2017

1 reference