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UnknownSoy-Based Infant Formula is Associated with an Increased Prevalence of Comorbidities in Fragile X Syndrome.
Not available
S-EPMC7602206 | biostudies-literature
UnknownImplications of the choroid plexus in Niemann-Pick disease Type C neuropathogenesis.
Not available
S-EPMC11787871 | biostudies-literature
UnknownEfficacy results from a 12-month double-blind randomized trial of arimoclomol for treatment of Niemann-Pick disease type C (NPC): Presenting a rescored 4-domain NPC Clinical Severity Scale.
Not available
S-EPMC12166820 | biostudies-literature
UnknownLongitudinal Characterization of Males With X-Linked Creatine Transporter Deficiency: Final Results of a Multiyear Observational Study.
Not available
S-EPMC12905711 | biostudies-literature
UnknownMutation update for the SATB2 gene.
Not available
S-EPMC11431158 | biostudies-literature
UnknownSPARK: A US Cohort of 50,000 Families to Accelerate Autism Research.
Not available
S-EPMC7444276 | biostudies-literature
UnknownLarge-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Not available
S-EPMC7530681 | biostudies-literature
UnknownExome sequencing of 457 autism families recruited online provides evidence for autism risk genes.
Not available
S-EPMC6707204 | biostudies-literature
UnknownIntegrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Not available
S-EPMC9470534 | biostudies-literature
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