Associated Papers
Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).
Bramswig NC et al.
Human Genetics, 2018
Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort.
Baronas K et al.
Acta Medica Lituanic, 2018
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