Marque, M <br/><br/>
Novel FH mutation in a patient with cutaneous leiomyomatosis associated with cutis verticis gyrata, eruptive collagenoma and Charcot-Marie-Tooth disease.  [electronic resource] 

 -  The British journal of dermatology  Dec 2010 
 - 1337-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2133 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2133.2010.09912.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carcinoma, Renal Cell--genetics<br/>Charcot-Marie-Tooth Disease--genetics<br/>Collagen Diseases--genetics<br/>Fumarate Hydratase--genetics<br/>Genetic Predisposition to Disease<br/>Humans<br/>Leiomyomatosis--enzymology<br/>Male<br/>Mutation<br/>Scalp Dermatoses--genetics<br/>Sequence Analysis, DNA<br/>Skin Diseases--genetics<br/>Skin Neoplasms--enzymology<br/>Young Adult