Data
Bouveret R
Bouveret R
Schonrock N
Ramialison M
Doan T
de Jong D
Bondue A
Kaur G
Mohamed S
Fonoudi H
Chen C
Wouters M
Bhattacharya S
Plachta N
Dunwoodie SL
Chapman G
Blanpain C
Harvey RP
(2015)
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets
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https://www.gov.uk/government/publications/educational-excellence-everywhere
PubMed
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