Hasegawa, Kosei <br/><br/>
Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene.  [electronic resource] 

 -  Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology  Jan 2015 
 - 33-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0918-5739 
<br/><br/><label>Standard No.: </label>10.1297/cpe.24.33  doi