R E Schnur. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultChildChromosome DeletionChromosomes, Human, Pair 16Chromosomes, Human, Pair 9Fibroma/diagnosisFibroma/geneticsGTP Phosphohydrolases/geneticsGTPase-Activating ProteinsHumansInfantMosaicism/geneticsMutation/geneticsNail Diseases/diagnosisNail Diseases/geneticsPhenotypeProteins/geneticsTuberous Sclerosis/diagnosisTuberous Sclerosis/genetics
Substances: See more » GTPase-Activating ProteinsProteinsGTP Phosphohydrolases
Year: 1995 PMID: 7492142 DOI: 10.1001/archderm.131.12.1460
Source DB: PubMed Journal: Arch Dermatol ISSN: 0003-987X