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RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)
by
Syx, Delfien
,
Malfait, Fransiska
,
Van Laer, Lut
,
Hellemans, Jan
,
Hermanns-Lê, Trinh
,
Willaert, Andy
,
Benmansour, Abdelmajid
,
De Paepe, Anne
,
Verloes, Alain
Published in
Human genetics
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