Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort. [electronic resource]
Producer: 20190417Description: 427-435 p. digitalISSN:- 1435-232X
- Amino Acid Substitution
- Animals
- Asian People
- Axin Protein -- genetics
- Child
- Child, Preschool
- China
- Cohort Studies
- Female
- Gene Knockdown Techniques
- Heart Defects, Congenital -- genetics
- High-Throughput Nucleotide Sequencing
- Humans
- Infant
- Male
- Mice
- Mutation, Missense
- Wnt Signaling Pathway -- genetics
- Zebrafish -- genetics
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Publication Type: Clinical Trial; Journal Article
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