Gyrate Atrophy in 2 Siblings – Ophthalmological Findings and A New Mutation-Reference-Cited by-同舟云学术

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Gyrate Atrophy in 2 Siblings – Ophthalmological Findings and A New Mutation

Published:2015-08-10 Issue:05 Volume:227 Page:296-298
ISSN:0300-8630
Container-title:Klinische Pädiatrie
language:de
Short-container-title:Klin Padiatr

Author:

Michel M.¹,Blatsios G.²,Scholl-Bürgi S.¹,Entenmann A.¹,Wernstedt A.³,Zschocke A.¹,Pichler K.¹,Höller A.¹,Karall D.¹

Affiliation:

1. Department for Pediatrics, Pediatrics I, Medical University Innsbruck, Innsbruck, Austria

2. Deparment for Ophthalmology, Medical University Innsbruck, Innsbruck, Germany

3. Department for Clinical Genetics, Medical University Innsbruck, Innsbruck, Austria

Publisher

Georg Thieme Verlag KG

Subject

Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1555921.pdf

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy;Journal of Ophthalmic and Vision Research;2024-03-10

2. A review of treatment modalities in gyrate atrophy of the choroid and retina (GACR);Molecular Genetics and Metabolism;2021-09

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