Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome is a research paper published in Human Molecular Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 42 times.
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Wellcome Trust
Grant: # 099175/Z/12/Z
Health Innovation Challenge Fund
Grant: HICF-1009-003
Wellcome Sanger Institute
Grant: WT098051
NIH
Grant: DK099478
NCATS NIH HHS
Grant: UL1 TR001863
Biotechnology and Biological Sciences Research Council
Grant: BB/R015953/1
Wellcome Trust
Grant: 099175/Z/12/Z
NIDDK NIH HHS
Grant: R01 DK099478
British Heart Foundation
Medical Research Council
Wellcome Trust
FWCI
2.31
Citation Percentile
0.9%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals