Maass, Philipp G <br/><br/>
PDE3A mutations cause autosomal dominant hypertension with brachydactyly.  [electronic resource] 

 -  Nature genetics  Jun 2015 
 - 647-53 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>1546-1718 
<br/><br/><label>Standard No.: </label>10.1038/ng.3302  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>Brachydactyly--genetics<br/>Case-Control Studies<br/>Cell Differentiation<br/>Child<br/>Cyclic Nucleotide Phosphodiesterases, Type 3--genetics<br/>Female<br/>Genetic Association Studies<br/>HeLa Cells<br/>Humans<br/>Hypertension--congenital<br/>Kinetics<br/>Male<br/>Mesenchymal Stem Cells--physiology<br/>Mice<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Myocytes, Smooth Muscle--physiology<br/>Pedigree