A novel HSPG2 splice site mutation causing Schwartz-Jampel syndrome is associated with an impaired lacunocanalicular system

A novel HSPG2 splice site mutation causing Schwartz-Jampel syndrome is associated with an impaired lacunocanalicular system

Bibliographic Details
Main Authors: Simon von Kroge, Uwe Kornak, Michaela Schweizer, Ralf Oheim, Michael Amling, Tim Rolvien
Format: Article
Language:English
Published: Elsevier 2020-10-01
Series:Bone Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S235218722030440X

Internet

http://www.sciencedirect.com/science/article/pii/S235218722030440X

Similar Items