Liu et al., 2018 - Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects. Genome Medicine   10:40 Full text @ Genome Med.
Morpholino List (7 Records)
Target Reagent
cfap46 MO1-linc.cfap46
dnah10 MO1-dnah10
galnt11 MO2-galnt11
linc.cfap46 MO1-linc.cfap46
numb MO5-numb
pacrg MO1-pacrg
rnf115a MO1-rnf115a
tctn2 MO1-tctn2
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