Associated Papers
Analysing an allelic series of rare missense variants of CACNA1I in a Swedish schizophrenia cohort.
Baez-Nieto D et al.
Brain : a Journal of Neurology, 2022
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease.
Izarzugaza JMG et al.
Genome Medicine, 2020
32859249 (PubMed )
Supplement: 13073_2020_772_MOESM1_ESM.pdf
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