Functional characterization of novel mutations inGNPAT andAGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3

dc.creatorItzkovitz, Brandon
dc.creatorJiralerspong, Sarn
dc.creatorNimmo, Graeme
dc.creatorLoscalzo, Melissa
dc.creatorHorovitz, Dafne Dain Gandelman
dc.creatorSnowden, Ann
dc.creatorMoser, Ann
dc.creatorSteinberg, Steve
dc.creatorBraverman, Nancy
dc.date.accessioned2014-12-22T17:47:57Z
dc.date.accessioned2023-09-05T13:14:32Z
dc.date.available2014-12-22T17:47:57Z
dc.date.available2023-09-05T13:14:32Z
dc.date.created2014-12-22T17:47:57Z
dc.date.issued2012
dc.identifierITZKOVITZ, Brandon et al. Functional characterization of novel mutations inGNPAT andAGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3. Human Mutation, New York, v. 33, n. 1, p. 189-197, 2012.
dc.identifier1059-7794
dc.identifierhttps://www.arca.fiocruz.br/handle/icict/9283
dc.identifier10.1002/humu.21623
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8657415
dc.languageeng
dc.publisherWiley-Liss
dc.rightsrestricted access
dc.titleFunctional characterization of novel mutations inGNPAT andAGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3
dc.typeArticle


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