Sturge Weber syndrome and rod cone dystrophy-Reference-Cited by-同舟云学术

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Sturge Weber syndrome and rod cone dystrophy

Published:2023-08-12 Issue: Volume: Page:
ISSN:1460-2725
Container-title:QJM: An International Journal of Medicine
language:en
Short-container-title:

Author:

Ganne P¹²^ORCID,Mootha V V²³,Mahindrakar A²^ORCID,Adusumilli H²

Affiliation:

1. Department of Ophthalmology, AIIMS, Mangalagiri , Guntur, Andhra Pradesh, India

2. Srikiran Institute of Ophthalmology , Kakinada, Andhra Pradesh, India

3. Department of Ophthalmology, University of Texas Southwestern Medical Center , Dallas, TX, USA

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Link

https://academic.oup.com/qjmed/advance-article-pdf/doi/10.1093/qjmed/hcad190/51238690/hcad190.pdf

Reference5 articles.

1. Sturge-Weber syndrome associated with other abnormalities: a medical record and literature review;Comi;Arch Neurol,2005

2. Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families;Bayés;Hum Genet,1995

3. A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13;Balciuniene;Genomics,1995

4. Retinitis pigmentosa associated with Sturge-Weber syndrome;Berkow;Arch Ophthalmol,1966

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