Digenic Inheritance of a FOXC2 Mutation and Two PIEZO1 Mutations Underlies Congenital Lymphedema in a Multigeneration Family
AMERICAN JOURNAL OF MEDICINE（2022）
Key words
Digenic inheritance,Familial lymphedema,FOXC2,Genotype-phenotype correlations,Jaundice,Lymphangioscintigraphy,PIEZO1
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined