Exome sequencing identifies truncating mutations in human SE…
Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta
Article, Chapter
Full text availability for this item
Collection:
Elsevier ScienceDirect Journals
Coverage:
- 1997-06~present
Collection:
Cell Press
Coverage:
- 1997-06~present
Collection:
PubMed Central
Coverage:
- 1949~6 months ago