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UnknownGenes and genetic testing in hereditary ataxias.
Not available
S-EPMC4198919 | biostudies-literature
UnknownPRICKLE2 Mutations Might Not Be Involved in Epilepsy.
Not available
S-EPMC4800039 | biostudies-literature
UnknownGenetic analysis of 20 patients with hypomyelinating leukodystrophy by trio-based whole-exome sequencing.
Not available
S-EPMC8310791 | biostudies-literature
UnknownHomozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome.
Not available
S-EPMC4276403 | biostudies-literature
UnknownEffects of the serotonin transporter gene, sensitivity of response to alcohol, and parental monitoring on risk for problem alcohol use.
Not available
S-EPMC5340078 | biostudies-literature
UnknownFIBCD1 is an endocytic GAG receptor associated with a novel neurodevelopmental disorder
Not available
S-SCDT-EMM-2022-15829 | biostudies-other
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