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UnknownHuman CRY1 variants associate with attention deficit/hyperactivity disorder.
Not available
S-EPMC7324179 | biostudies-literature
UnknownGPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates.
Not available
S-EPMC6748651 | biostudies-literature
UnknownEstablishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project.
Not available
S-EPMC10547150 | biostudies-literature
UnknownAssociation of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.
Not available
S-EPMC8406220 | biostudies-literature
UnknownGenome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Not available
S-EPMC5867896 | biostudies-literature
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