Carl Fratter

5PUBLICATIONS
18CO-AUTHORS
Cell and nuclear divisionMedical molecular engineering of nucleic acids and proteinsGene and molecular therapyEpigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)
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Publications (5)

|Dec 13, 2022
Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines.

Eleni Mavraki, Robyn Labrum, Kate Sergeant

|Jul 24, 2020
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans.

Wei Wei, Alistair T Pagnamenta, Nicholas Gleadall

|May 20, 2020
EMQN best practice guidelines for genetic testing in dystrophinopathies.

Carl Fratter, Raymond Dalgleish, Stephanie K Allen

|Apr 10, 2020
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans.

Wei Wei, Alistair T Pagnamenta, Nicholas Gleadall

|Aug 30, 2019
The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency.

Nandaki Keshavan, Jose Abdenur, Glenn Anderson

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Frequent Collaborators

3 joint publications

Shamima Rahman

2 joint publications

Mark J Caulfield

2 joint publications

Ernest Turro

2 joint publications

Salih Tuna