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Publications by Holger Prokisch
NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals With Leigh-Like Encephalomyopathy
American Journal of Human Genetics
Genetics
Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis
American Journal of Human Genetics
Genetics
CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
American Journal of Human Genetics
Genetics
Bi-Allelic ADPRHL2 Mutations Cause Neurodegeneration With Developmental Delay, Ataxia, and Axonal Neuropathy
American Journal of Human Genetics
Genetics
RINT1 Bi-Allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities
American Journal of Human Genetics
Genetics
OUTRIDER: A Statistical Method for Detecting Aberrantly Expressed Genes in RNA Sequencing Data
American Journal of Human Genetics
Genetics
Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome
American Journal of Human Genetics
Genetics
Mitochondrial Replacement Approaches: Challenges for Clinical Implementation
Genome Medicine
Molecular Medicine
Genetics
Molecular Biology
Mutation in ITCH Gene Can Cause Syndromic Multisystem Autoimmune Disease With Acute Liver Failure
Pediatrics
Child Health
Pediatrics
Perinatology
The Metabolic Network Coherence of Human Transcriptomes Is Associated With Genetic Variation at the Cadherin 18 Locus
Human Genetics
Genetics
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