Ontology highlight
ABSTRACT:
SUBMITTER: Yahia A
PROVIDER: S-EPMC8021710 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature
Yahia Ashraf A Stevanin Giovanni G
Frontiers in genetics 20210323
Hereditary spinocerebellar degeneration (SCD) encompasses an expanding list of rare diseases with a broad clinical and genetic heterogeneity, complicating their diagnosis and management in daily clinical practice. Correct diagnosis is a pillar for precision medicine, a branch of medicine that promises to flourish with the progressive improvements in studying the human genome. Discovering the genes causing novel Mendelian phenotypes contributes to precision medicine by diagnosing subsets of patie ...[more]