Scott et al., 2017 - Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein. PLoS Genetics   13:e1006936 Full text @ PLoS Genet.
6 Genes / Markers
Marker Type Symbol Name
Gene hsp70l heat shock cognate 70-kd protein, like
Gene mkks MKKS centrosomal shuttling protein
Gene myl7 myosin, light chain 7, regulatory
Gene nkx2.5 NK2 homeobox 5
Gene nppa natriuretic peptide A
Gene smarcc1a SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1a
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