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

Delfien Syx; Fransiska Malfait; Lut Van Laer; Jan Hellemans; Trinh Hermanns-Lê; Andy Willaert; Abdelmajid Benmansour; Anne De Paepe; Alain Verloes
Human Genetics · Vol. 128, Issue 1 · pp. 79-88 · 2010
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2010-07-01
Publication Year2010
Volume128
Issue1
Pages79-88
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-010-0829-0

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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