PITX2 deficiency and associated human disease: insights from the zebrafish model-Reference-Cited by-同舟云学术

PITX2 deficiency and associated human disease: insights from the zebrafish model

Published:2018-03-01 Issue:10 Volume:27 Page:1675-1695
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Hendee Kathryn E¹²,Sorokina Elena A¹,Muheisen Sanaa S¹,Reis Linda M¹,Tyler Rebecca C¹,Markovic Vujica³⁴,Cuturilo Goran³⁵,Link Brian A²⁶,Semina Elena V¹²⁶

Affiliation:

1. Department of Pediatrics and Children’s Research Institute Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, WI 53226, USA

2. Department of Cell Biology, Neurobiology, and Anatomy, Medical College of Wisconsin, Milwaukee, WI 53226, USA

3. Faculty of Medicine, University of Belgrade, Serbia

4. Clinical Centre of Serbia, University Eye Hospital, Belgrade, Serbia

5. Department of Medical Genetics, University Children’s Hospital, Belgrade, Serbia

6. Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, WI 53226, USA

Funder

National Institutes of Health

NIH

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/27/10/1675/25087147/ddy074.pdf

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3. PITX2 and FOXC1 spectrum of mutations in ocular syndromes;Reis;Eur. J. Hum. Genet,2012

4. Axenfeld-Rieger syndrome in the age of molecular genetics;Alward;Am. J. Ophthalmol,2000

5. Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations;Strungaru;Invest. Ophthalmol. Vis. Sci,2007

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