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Publications by Henrik Stranneheim
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
Medicine
Genetics
Pharmacology
Design and Assessment of Binary DNA for Nanopore Sequencing
Genome Biology
Related publications
Identification of a Novel TTC19 Mutation in a Portuguese Family With Complex III Deficiency
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
BCS1L Gene Mutation Causing GRACILE Syndrome: Case Report
Renal Failure
Medicine
Nephrology
Critical Care
Intensive Care Medicine
Barrier Abnormality Due to Ceramide Deficiency Leads to Psoriasiform Inflammation in a Mouse Model
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
A Novel Mutant Mouse, Joggle, With Inherited Ataxia
Experimental Animals
Genetics
Molecular Biology
Biochemistry
Veterinary
Animal Science
Medicine
Zoology
NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals With Leigh-Like Encephalomyopathy
American Journal of Human Genetics
Genetics
Respiratory Chain Deficiency in Nonmitochondrial Disease
Neurology: Genetics
Neurology
Genetics
Isolated Complex III Deficiency
How to Phenotype a Mouse
DMM Disease Models and Mechanisms
Immunology
Molecular Biology
Biochemistry
Microbiology
Neuroscience
Medicine
Genetics
Histological and Behavioral Phenotypes of a Novel Mutated APP Knock-In Mouse
Journal of Alzheimer's Disease
Gerontology
Clinical Psychology
Mental Health
Psychiatry
Geriatrics
Medicine
Neuroscience
