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Publications by F Möller
Gene-Based Treatment Options for Usher Type 1C by Translational Read-Through of a Nonsense Mutation
Cilia
Cell Biology
Related publications
Gene Repair of an Usher Syndrome Causing Mutation by Zinc-Finger Nuclease Mediated Homologous Recombination
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Neurofilament Deficiency in Quail Caused by Nonsense Mutation in Neurofilament-L Gene
Journal of Cell Biology
Medicine
Cell Biology
Nonsense Mutation of Islet-1 Gene (Q310X) Found in a Type 2 Diabetic Patient With a Strong Family History
Diabetes
Internal Medicine
Endocrinology
Metabolism
Diabetes
Identification of a Nonsense Mutation in the PAX9 Gene in Molar Oligodontia
European Journal of Human Genetics
Genetics
Lentiviral Gene Replacement Therapy of Retinas in a Mouse Model for Usher Syndrome Type 1B
Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
Profound, Prelingual Nonsyndromic Deafness Maps to Chromosome 10q21 and Is Caused by a Novel Missense Mutation in the Usher Syndrome Type IF Gene PCDH15
European Journal of Human Genetics
Genetics
Read-Through Strategies for Suppression of Nonsense Mutations in Duchenne/ Becker Muscular Dystrophy: Aminoglycosides and Ataluren (PTC124)
Journal of Child Neurology
Child Health
Neurology
Pediatrics
Perinatology
A Nonsense Mutation in a Cinnamyl Alcohol Dehydrogenase Gene Is Responsible for the Sorghum Brown Midrib6 Phenotype
Plant Physiology
Plant Science
Genetics
Physiology
Severe Cystic Fibrosis in a Child Homozygous for the G542 Nonsense Mutation in the CFTR Gene.
Journal of Medical Genetics
Genetics
