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Publications by Christoph Freyer

Neu-Laxova Syndrome Is a Heterogeneous Metabolic Disorder Caused by Defects in Enzymes of the L-Serine Biosynthesis Pathway

American Journal of Human Genetics

Genetics

2014

English

Mitochondrial Polyadenylation Is a One-Step Process Required for mRNA Integrity and tRNA Maturation

English

Absence of TXNIP in Human Gives Lactic Acidosis and Low Serum Methionine Linked to Deficient Respiration on Pyruvate

English

Metabolic Regulation of Neurodifferentiation in the Adult Brain

Cellular and Molecular Life Sciences

Molecular Neuroscience

English

Respiratory Chain Complex III Deficiency Due to Mutated BCS1L: A Novel Phenotype With Encephalomyopathy, Partially Phenocopied in a Bcs1l Mutant Mouse Model

Orphanet Journal of Rare Diseases

English

Mutations in the Mitochondrial Tryptophanyl‐tRNA Synthetase Cause Growth Retardation and Progressive Leukoencephalopathy

Molecular genetics & genomic medicine

Genetics

Molecular Biology

2019

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Christoph Freyer

Neu-Laxova Syndrome Is a Heterogeneous Metabolic Disorder Caused by Defects in Enzymes of the L-Serine Biosynthesis Pathway

Mitochondrial Polyadenylation Is a One-Step Process Required for mRNA Integrity and tRNA Maturation

Absence of TXNIP in Human Gives Lactic Acidosis and Low Serum Methionine Linked to Deficient Respiration on Pyruvate

Metabolic Regulation of Neurodifferentiation in the Adult Brain

Respiratory Chain Complex III Deficiency Due to Mutated BCS1L: A Novel Phenotype With Encephalomyopathy, Partially Phenocopied in a Bcs1l Mutant Mouse Model

Mutations in the Mitochondrial Tryptophanyl‐tRNA Synthetase Cause Growth Retardation and Progressive Leukoencephalopathy