Work

βA3/A1-crystallin and persistent fetal vasculature (PFV) disease of the eye

Year: 2015

Type: article

Source: Biochimica et Biophysica Acta (BBA) - General Subjects

DOI: 10.1016/j.bbagen.2015.05.017

Authors: J. Samuel Zigler, Mallika Valapala, Peng Shang, Stacey Hose, Morton F. Goldberg, Debasish Sinha

Institutions: Johns Hopkins University, Johns Hopkins Medicine, Tongji University

Language: English

Topic: Ocular Disorders and Treatments

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Foundation for the National Institutes of Health, Knights Templar Eye Foundation, Research to Prevent Blindness, National Institutes of Health, National Eye Institute

Awards: A novel bA3/A1-crystallin gene mutation results in persistent fetal vasculature, G1582333981, G1885968165, A CRYSTALLIN MUTATION WITH ABNORMAL ASTROCYTES AND RETINAL VESSELS, G2795717175, G3033057233, G3773112255, G4716643746, G5059618418, P30 Wilmer Core Grant for Vision Research, G6461947084, G6517750212, G9000169224

OpenAlex ID: W429548527

FWCI: 1.027

Cites: 75

Cited by: 24

Related to: 10