Work

Leber congenital amaurosis with early-onset severe macular atrophy and optic atrophy is likely pathognomonic of NMNAT1 mutations

Year: 2015

Type: article

Source: Investigative Ophthalmology & Visual Science

Authors: Olivia Xerri, Isabelle Perrault, Sylvain Hanein, Nathalie Delphin, Lucas Fares‐Taie, S. Gerber, Olivier Roche, Arnold Münnich, Josseline Kaplan, Jean‐Michel Rozet

Institutions: Institut des Maladies Génétiques Imagine, Hôpital Necker-Enfants Malades

Language: English

Topic: Retinal Development and Disorders

Subfield: Ophthalmology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2139156992

FWCI:

Cites:

Cited by:

Related to: 10