Chrome Extension
WeChat Mini Program
Use on ChatGLM

New Structural and Single Nucleotide Mutations in Type I and Type II Collagens in Taiwanese Children with Type I and Type II Collagenopathies

FRONTIERS IN GENETICS(2021)

Cited 1|Views7
Key words
osteogenesis imperfecta,spondyloepiphyseal dysplasia congenita,collagen,osteoporosis,next-generation sequencing
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