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Publications by Richard I. Kelley
Mutations in the Human SC4MOL Gene Encoding a Methyl Sterol Oxidase Cause Psoriasiform Dermatitis, Microcephaly, and Developmental Delay
Journal of Clinical Investigation
Medicine
Severity of Cardiomyopathy Associated With Adenine Nucleotide Translocator-1 Deficiency Correlates With mtDNA Haplogroup
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome
American Journal of Human Genetics
Genetics
Mitochondrial Disease in Autism Spectrum Disorder Patients: A Cohort Analysis
PLoS ONE
Multidisciplinary