Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies-Reference-Cited by-同舟云学术

Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies

Author:

Reis L. M.¹,Tyler R. C.¹,Weh E.¹²,Hendee K. E.¹²,Schilter K. F.¹²,Phillips J. A.³,Sequeira S.⁴,Schinzel A.⁵,Semina E. V.¹²⁶

Affiliation:

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

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

3. Division of Medical Genetics and Genomic Medicine; Vanderbilt University Medical Center; Nashville TN USA

4. Metabolic Unit, Pediatric Department; Hospital de Dona Estefânia, CHLC; Lisbon Portugal

5. Department of Genetics; Institute of Medical Genetics; Schwerzenbach Switzerland

6. Department of Ophthalmology; Medical College of Wisconsin; Milwaukee WI USA

Funder

National Eye Institute

Children's Research Institute Foundation at Children's Hospital of Wisconsin

Institute Core Facilities

National Institutes of Health

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference11 articles.

2. Role of CYP1B1 in glaucoma;Vasiliou;Annu Rev Pharmacol Toxicol,2008

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