A mosaic activating mutation in AKT1 associated with the Proteus syndrome. [electronic resource]
- The New England journal of medicine Aug 2011
- 611-9 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
1533-4406
10.1056/NEJMoa1104017 doi
Child DNA Mutational Analysis Exons--genetics Genotype Humans Male Mosaicism Mutation Phosphorylation Proteus Syndrome--genetics Proto-Oncogene Proteins c-akt--genetics