Boudin, Eveline <br/><br/>
No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disorders.  [electronic resource] 

 -  Bone  Jul 2013 
 - 52-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1873-2763 
<br/><br/><label>Standard No.: </label>10.1016/j.bone.2013.03.015  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Bone Diseases--genetics<br/>Bone and Bones--pathology<br/>DNA Mutational Analysis<br/>Gene Frequency--genetics<br/>Humans<br/>Mice<br/>Mutation--genetics<br/>Nucleotides--genetics<br/>Receptor, Serotonin, 5-HT1B--genetics<br/>Sclerosis--genetics<br/>Serotonin--genetics<br/>Tryptophan Hydroxylase--genetics