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Publications by G. A. F. Nicolaes
Two Novel Mutations in the SLC25A4 Gene in a Patient With Mitochondrial Myopathy
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Related publications
Two Novel Mutations of the CYP11B2 Gene in a Japanese Patient With Aldosterone Deficiency Type 1
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family With Autosomal Dominant Mitochondrial Myopathy
Neurogenetics
Molecular Neuroscience
Genetics
Cellular
Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Mitochondrial Myopathy in Follow-Up of a Patient With Chronic Fatigue Syndrome
Journal of Investigative Medicine High Impact Case Reports
Risk
Epidemiology
Reliability
Safety
Safety Research
Quality
A Novel De Novo Dominant Mutation inISCUassociated With Mitochondrial Myopathy
Journal of Medical Genetics
Genetics
Three Novel Mutations in the Glycoprotein IIb Gene in a Patient With Type II Glanzmann Thrombasthenia
Haematologica
Hematology
Manometrical Study of the Upper Esophagus in Two Cases With Mitochondrial Myopathy.
Nihon Kikan Shokudoka Gakkai Kaiho
Identification of Two Novel LAMA2 Mutations in a Chinese Patient With Congenital Muscular Dystrophy
Frontiers in Genetics
Genetics
Molecular Medicine
Novel Point Mutations in Mitochondrial 16S rRNA Gene of Chinese Hamster Cells.
Genes and Genetic Systems
Medicine
Genetics
Molecular Biology