Retinal Pathology in GM1 Gangliosidosis, Type II-Reference-Cited by-同舟云学术

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Retinal Pathology in GM1 Gangliosidosis, Type II

Published:1973-03 Issue:3 Volume:75 Page:434-441
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Goebel Hans H.,Fix James D.,Zeman Wolfgang

Publisher

Elsevier BV

Subject

Ophthalmology

Reference15 articles.

1. Heritable Disorders of Connective Tissue;McKusick,1966

2. Tay-Sachs' retina: Deficiency of acetyl hexosaminidase A;Cotlier;Arch. Ophth.,1971

3. Symmetrical changes in the region of the yellow spot in each eye of an infant;Tay;Trans. Ophth. Soc. U.K.,1881

4. The neuronal ceroid-lipofuscinoses (Batten-Vogt syndrome);Zeman,1970

5. The sphin-golipidoses and the eye;Cogan;Arch. Ophth.,1968

Cited by 19 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. GM1 Gangliosidosis: Mechanisms and Management;The Application of Clinical Genetics;2021-04

2. Lysosomal storage diseases;Translational Science of Rare Diseases;2017-05-25

3. Lysosomal Storage Diseases;2017

4. Metabolic Diseases;Pediatric Ophthalmology and Strabismus;2003

5. Manifestation of infantile GM1 gangliosidosis in the fetal eye;Graefe's Archive for Clinical and Experimental Ophthalmology;1988-01

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