(Q35569356)

8 August 2017

Leber's optic atrophy, a possible example of maternal inheritance. (English)

1 reference

8 August 2017

1 reference

Erickson RP

1

1 reference

PubMed ID

5063796

8 August 2017

language of work or name

English

0 references

publication date

1 May 1972

1 reference

American Journal of Human Genetics

8 August 2017

1 reference

8 August 2017

24

1 reference

8 August 2017

3

1 reference

8 August 2017

348-349

1 reference

Leber's hereditary optic atrophy: some clinical and aetiological considerations.

8 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762279

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762279

A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762279

Some remarks on the clinical and genetic puzzle of Leber's optic neuritis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762279

Uptake of heterologous genome by mammalian spermatozoa and its transfer to ova through fertilization

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762279

An analysis of natural scrapie in suffolk sheep

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762279

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762279

26 September 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/5063796

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Anencephaly and Spina Bifida: a Possible Example of Cytoplasmic Inheritance in Man

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/5063796

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Low density lipoprotein peptide metabolism in nephrotic syndrome: a comparison with patterns observed in other syndromes characterised by hyperlipoproteinaemia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/5063796

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1762279

1 reference

8 August 2017

1 reference

PubMed ID

5063796