List of works - Andrew A Morris

A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndrome

scientific article published in June 2004

A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype

scientific article published on 18 April 2016

A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency

scientific article

Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder

scientific article published on 16 February 2018

Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene

scientific article

Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy

article

LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population.

scientific article published on 27 October 2015

Leigh syndrome caused by mutations in is associated with a better prognosis

article

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.

scientific article published on 24 February 2018

Maternally inherited mitochondrial DNA disease in consanguineous families

scientific article published on 29 June 2011

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation

scientific article published on 22 January 2002

Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits

scientific article published on 26 October 2017

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies

scientific article

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies

article

SURF1 deficiency: a multi-centre natural history study.

scientific article published on 05 July 2013

The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease.

scientific article published on 13 July 2016

The genotypic and phenotypic spectrum of MTO1 deficiency.

scientific article published on 15 November 2017

Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.

scientific article published in July 2014

List of works by Andrew A Morris

A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndrome

A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype

A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency

Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder

Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene

Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy

LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population.

Leigh syndrome caused by mutations in is associated with a better prognosis

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.

Maternally inherited mitochondrial DNA disease in consanguineous families

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation

Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies

SURF1 deficiency: a multi-centre natural history study.

The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease.

The genotypic and phenotypic spectrum of MTO1 deficiency.

Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.