<scp>GGC</scp> Repeat Expansion of <scp> <i>RILPL1</i> </scp> is Associated with Oculopharyngodistal Myopathy-Reference-Cited by-同舟云学术

GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy

Published:2022-07-02 Issue:3 Volume:92 Page:512-526
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Annals of Neurology

Author:

Zeng Yi‐Heng¹,Yang Kang¹,Du Gan‐Qin²,Chen Yi‐Kun¹^ORCID,Cao Chun‐Yan²,Qiu Yu‐Sen¹,He Jin¹^ORCID,Lv Hai‐Dong³,Qu Qian‐Qian³,Chen Jian‐Nan⁴,Xu Guo‐Rong¹,Chen Long¹,Zheng Fu‐Ze¹,Zhao Miao¹,Lin Min‐Ting¹,Chen Wan‐Jin¹^ORCID,Hu Jing⁴,Wang Zhi‐Qiang¹,Wang Ning¹^ORCID

Affiliation:

1. Department of Neurology and Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology Fujian Medical University Fuzhou China

2. The First Affiliated Hospital College of Clinical Medicine of Henan University of Science and Technology Luoyang China

3. Department of Neurology The People's Hospital of Jiaozuo City Jiaozuo China

4. Department of Neuromuscular Disorders The Third Hospital of Hebei Medical University Shijiazhuang China

Funder

Natural Science Foundation of Fujian Province

National Natural Science Foundation of China

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.26436

Reference45 articles.

1. Oculopharyngodistal Myopathy

2. Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity

3. Oculopharyngodistal myopathy is a distinct entity: Clinical and genetic features of 47 patients

4. Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

5. Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy

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