ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome

J Žák; V Vives; D Szumska; A Vernet; J E Schneider; P Miller; E A Slee; S Joss; Y Lacassie; E Chen; L F Escobar; M Tucker; A S Aylsworth; H A Dubbs; A T Collins; J Andrieux; A Dieux-Coeslier; E Haberlandt; D Kotzot; D A Scott; M J Parker; Z Zakaria; Y S Choy; D Wieczorek; A M Innes; K R Jun; S Zinner; F Prin; C A Lygate; P Pretorius; J A Rosenfeld; T J Mohun; X Lu

doi:10.1038/cdd.2016.76

journal article Jul 22, 2016

ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome

V Vives D Szumska A Vernet J E Schneider P Miller E A Slee S Joss Y Lacassie E Chen L F Escobar M Tucker A S Aylsworth H A Dubbs A T Collins J Andrieux A Dieux-Coeslier E Haberlandt D Kotzot D A Scott M J Parker Z Zakaria Y S Choy D Wieczorek A M Innes K R Jun S Zinner F Prin C A Lygate P Pretorius J A Rosenfeld T J Mohun X Lu

Cell Death & Differentiation Vol. 23 No. 12 pp. 1973-1984 · Springer Science and Business Media LLC

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Published: Jul 22, 2016
Vol/Issue: 23(12)
Pages: 1973-1984
License: View

Authors

J

J Žák

Astronomical Institute, Czech Academy of Sciences , Fričova 298, 251 65 Ondřejov ,

for the Genetics in Glaucoma Patients of African Descent (GIGA) Study GroupGenetics of Glaucoma in People of African Descent (GGLAD) Study GroupMillion Veteran Program (MVP)

Department of Microbiology, Vanderbilt University Medical School, Nashville, Tennessee 37232-2581, USA.

Cite This Article

J Žák, V Vives, D Szumska, et al. (2016). ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome. Cell Death & Differentiation, 23(12), 1973-1984. https://doi.org/10.1038/cdd.2016.76

ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome

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