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Publications by Oliver Stehling

A Novel De Novo Dominant Mutation inISCUassociated With Mitochondrial Myopathy

Journal of Medical Genetics

English

Cellular Requirements for Iron–sulfur Cluster Insertion Into the Antiviral Radical SAM Protein Viperin

Journal of Biological Chemistry

Molecular Biology

English

Related publications

Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family With Autosomal Dominant Mitochondrial Myopathy

Molecular Neuroscience

English

A Novel De Novo Dominant Mutation of NOTCH1 Gene in an Iranian Family With Non‐syndromic Congenital Heart Disease

Journal of Clinical Laboratory Analysis

Medical Laboratory Technology

Clinical Biochemistry

Occupational Health

English

GNE Myopathy in Turkish Sisters With a Novel Homozygous Mutation

Case Reports in Neurological Medicine

English

A Novel De Novo Mutation in CEACAM16 Associated With Postlingual Hearing Impairment

Molecular Syndromology

English

A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy

American Journal of Human Genetics

English

Two Novel Mutations in the SLC25A4 Gene in a Patient With Mitochondrial Myopathy

Internal Medicine

Molecular Biology

English

A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

English

A Novel De Novo COL1A1 Mutation in a Thai Boy With Osteogenesis Imperfecta Born to Consanguineous Parents

Genetics and Molecular Biology

Molecular Biology

English

A Patient With a Novel Gene Mutation Leading to Autosomal Dominant Polycystic Kidney Disease

Clinical Journal of the American Society of Nephrology

Transplantation

Intensive Care Medicine

English