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UnknownImpairment of Motor Function Correlates with Neurometabolite and Brain Iron Alterations in Parkinson's Disease.
Not available
S-EPMC6406520 | biostudies-literature
UnknownDe novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.
Not available
S-EPMC7007577 | biostudies-literature
UnknownEvidence for 28 genetic disorders discovered by combining healthcare and research data.
Not available
S-EPMC7116826 | biostudies-literature
UnknownGenomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland.
Not available
S-EPMC7614484 | biostudies-literature
UnknownBiallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Not available
S-EPMC10932913 | biostudies-literature
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