A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human-Reference-Cited by-同舟云学术

A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human

Author:

Madelaine Romain¹,Notwell James H²,Skariah Gemini¹,Halluin Caroline¹,Chen Charles C²,Bejerano Gill²³⁴,Mourrain Philippe¹⁵

Affiliation:

1. Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA

2. Department of Computer Science, Stanford, CA 94305, USA

3. Department of Developmental Biology, Stanford, CA 94305, USA

4. Division of Medical Genetics, Department of Pediatrics, Stanford, CA 94305, USA

5. INSERM 1024, Ecole Normale Supérieure Paris, 75005, France

Funder

National Institute of Health

EMBO Long Term Fellowship

National Science Foundation Fellowship

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

Reference71 articles.

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