The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)
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J. Hellemans | A. Verloes | A. Willaert | A. Paepe | F. Malfait | T. Hermanns‐Lê | D. Syx | L. Laer | Abdelmajid Benmansour | Delfien Syx