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2025-06-25T03:06:11
RDF description of American Journal of Human Genetics - http://repository.healthpartners.com/individual/journal-American-Journal-of-Human-Genetics
journal-American-Journal-of-Human-Genetics
Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region
MECR mutations cause childhood-onset dystonia and optic atrophy, a mitochondrial fatty acid synthesis disorder
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations [meta-analysis]
American Journal of Human Genetics
Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study
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