Clinical and genetic characteristics of type I sialidosis patients in mainland China-Reference-Cited by-同舟云学术

Clinical and genetic characteristics of type I sialidosis patients in mainland China

Published:2020-05-29 Issue:6 Volume:7 Page:911-923
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Lv Rui‐Juan¹^ORCID,Li Tao‐Ran¹²^ORCID,Zhang Yu‐Di¹³^ORCID,Shao Xiao‐Qiu¹^ORCID,Wang Qun¹^ORCID,Jin Li‐Ri⁴^ORCID

Affiliation:

1. Department of Neurology Beijing Tiantan Hospital, Capital Medical University; China National Clinical Research Center for Neurological Diseases 119 South Fourth Ring West Road, Fengtai District Beijing 100070 PR. China

2. Department of Neurology Xuanwu Hospital of Capital Medical University 45 Chang Chun Road, Xicheng District Beijing 100053 PR. China

3. Department of Neurology the Second Hospital of Hebei Medical University, Hebei Medical University 215 Heping West Road, Xinhua District Hebei 050000 Shijiazhuang PR. China

4. Department of Neurology Peking Union Medical College Hospital Chinese Academy of Medical Sciences and Peking Union Medical College 1 Shuaifuyuan, Dongcheng District Beijing 100730 PR. China

Funder

the Application Research of Capital Clinical Characteristics

the Beijing Dongcheng District Outstanding Talent Funding Project

the National Key R&D Program of China

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.51058

Reference45 articles.

1. Mucolipidosis I: Increased sialic acid content and deficiency of an α-N-acetylneuraminidase in cultured fibroblasts

2. Sialidosis (mucolipidosis I);Durand P;Helv Paediatr Acta,1977

3. Mucolipidosis I — A sialidosis

4. Sialidoses

5. Sialidosis: A Review of Morphology and Molecular Biology of a Rare Pediatric Disorder

Cited by 1 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. Lysosomal storage disorders identified in adult population from India: Experience of a tertiary genetic centre and review of literature;JIMD Reports;2024-01-02