The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)

✍ Scribed by Delfien Syx; Fransiska Malfait; Lut Van Laer; Jan Hellemans; Trinh Hermanns-Lê; Andy Willaert; Abdelmajid Benmansour; Anne De Paepe; Alain Verloes

• Publisher: Springer
• Year: 2010
• Tongue: English
• Weight: 574 KB
• Volume: 128
• Category: Article
• ISSN: 0340-6717
• DOI: 10.1007/s00439-010-0829-0