Fingerprint
Dive into the research topics of 'C1q deficiency in an Inuit family: Identification of a new class of C1q disease-causing mutations'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
C1q deficiency in an Inuit family: Identification of a new class of C1q disease-causing mutations
Hanne Vibeke Marquart, Lone Schejbel, Anders Sjöholm, Ulla Mårtensson, Susan Nielsen, Anders Koch, Arne Svejgaard, Peter Garred
Research output: Contribution to journal › Article › peer-review