Work

A Novel FOXC1 Nonsense Mutation Is Associated With Sensorineural Hearing Loss, Primary Empty Sella Syndrome and Anterior Segment Dysgenesis

Year: 2007

Type: article

Source: Investigative Ophthalmology & Visual Science

Authors: Kevin Linkroum, E. DelBono, Michael J. McKenna, Janey L. Wiggs

Institution: Harvard 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: closed

OpenAlex ID: W1450808643

FWCI:

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Related to: 10