Abstract
Identification of novo mutations of NLRP7 in HM patients. NLRP7 mutations increasing the risk of HM progression.
© 2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Publication types
-
Letter
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Adaptor Proteins, Signal Transducing* / genetics
-
Female
-
Gestational Trophoblastic Disease* / pathology
-
Humans
-
Hydatidiform Mole* / genetics
-
Mutation
-
Pregnancy
Substances
-
Adaptor Proteins, Signal Transducing
-
NLRP7 protein, human