A NovelNDPMutation in an Infant with Unilateral Persistent Fetal Vasculature and Retinal Vasculopathy-Reference-Cited by-同舟云学术

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A NovelNDPMutation in an Infant with Unilateral Persistent Fetal Vasculature and Retinal Vasculopathy

Published:2009-01 Issue:2 Volume:30 Page:99-102
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Aponte Elisabeth P.,Pulido Jose S.,Ellison Jay W.,Quiram Polly A.,Mohney Brian G.

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1080/13816810802705755

Reference16 articles.

1. CAUSES OF BLINDNESS IN CHILDREN

2. A novel missense mutation in theNDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms

3. Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome

4. Norrie Disease Gene: Characterization of Deletions and Possible Function

5. The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3

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3. Pediatric retinal vascular disorders: From translational sciences to clinical practice;Saudi Journal of Ophthalmology;2023-10

4. First implication of MIP in bilateral microphthalmia with persistent fetal vasculature;American Journal of Medical Genetics Part A;2023-02-03

5. A Case of Unilateral Pseudoglioma of Eye in A Neonate;International Journal of Life Science and Pharma Research;2022-07-29

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