Clinical Characteristics and Genetic Variants in Taiwanese Patients With <i>PROM1</i>-Related Inherited Retinal Disorders-Reference-Cited by-全球学者库

Clinical Characteristics and Genetic Variants in Taiwanese Patients With PROM1-Related Inherited Retinal Disorders

Published:2023-11-17 Issue:14 Volume:64 Page:25
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Lin Tzu-Yi¹²,Wu Pei-Liang³⁴,Kang Eugene Yu-Chuan²⁴⁵⁶,Chi Yi-Chun⁷,Jenny Laura A.⁴,Lin Pei-Hsuan⁴⁸,Lee Chia-Ying⁵,Liu Chun-Hsiu²⁵,Liu Laura²⁵,Yeh Lung-Kun²⁵,Chen Kuan-Jen²⁵,Hwang Yih-Shiou²⁵,Wu Wei-Chi²⁵,Lai Chi-Chun²⁵⁹,Hsiao Meng-Chang¹⁰,Liu Pei-Kang⁷¹¹,Wang Nan-Kai²⁴⁵

Affiliation:

1. Department of Education, Chang Gung Memorial Hospital, Linkou Medical Center, Taoyuan, Taiwan

2. College of Medicine, Chang Gung University, Taoyuan, Taiwan

3. College of Medicine, National Taiwan University, Taipei, Taiwan

4. Department of Ophthalmology, Edward S. Harkness Eye Institute, Columbia University Irving Medical Center, Columbia University, New York, New York, United States

5. Department of Ophthalmology, Chang Gung Memorial Hospital, Linkou Medical Center, Taoyuan, Taiwan

6. Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan

7. Department of Ophthalmology, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan

8. Department of Ophthalmology, National Taiwan University Yunlin Branch, Yunlin, Taiwan

9. Department of Ophthalmology, Chang Gung Memorial Hospital, Keelung, Taiwan

10. Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, United States

11. School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

Cardiology and Cardiovascular Medicine

Reference39 articles.

1. A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration;Maw;Hum Mol Genet,2000

2. AC133, a novel marker for human hematopoietic stem and progenitor cells;Yin;Blood,1997

3. A novel five-transmembrane hematopoietic stem cell antigen: isolation, characterization, and molecular cloning;Miraglia;Blood,1997

4. Prominin, a novel microvilli-specific polytopic membrane protein of the apical surface of epithelial cells, is targeted to plasmalemmal protrusions of non-epithelial cells;Weigmann;Proc Natl Acad Sci USA,1997

5. Genetic identification and molecular modeling characterization reveal a novel PROM1 mutation in Stargardt4-like macular dystrophy;Imani;Oncotarget,2018

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