Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome.
Authors | Mateusz Kolanczyk, Peter Krawitz, Jochen Hecht, Anna Hupalowska, Marta Miaczynska, Katrin Marschner, Claire Schlack, Denise Emmerich, Karolina Kobus, Uwe Kornak, Peter N Robinson, Barbara Plecko, Gernot Grangl, Sabine Uhrig, Stefan Mundlos, Denise Horn |
Journal | European journal of human genetics : EJHG
(Eur J Hum Genet)
Vol. 23
Issue 5
Pg. 720
(May 2015)
ISSN: 1476-5438 [Electronic] England |
PMID | 25880334
(Publication Type: Published Erratum)
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