Hartnup disease presenting as hereditary spastic paraplegia and severe peripheral neuropathy-Reference-Cited by-同舟云学术

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Hartnup disease presenting as hereditary spastic paraplegia and severe peripheral neuropathy

Published:2021-08-30 Issue:1 Volume:188 Page:237-242
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Wang Xianling¹^ORCID,Li Xu‐Ying¹²^ORCID,Piao Yueshan¹³,Yuan Guobin¹,Lin Yicong¹,Chen Hai¹,Wang Zhanjun¹,Li Cunjiang¹,Wang Chaodong¹^ORCID

Affiliation:

1. Department of Neurology Xuanwu Hospital of Capital Medical University, National Clinical Research Center for Geriatric Diseases Beijing China

2. Institute of Genetics and Developmental Biology Chinese Academy of Sciences Beijing China

3. Department of Pathology Xuanwu Hospital of Capital Medical University Beijing China

Funder

Beijing Municipal Science and Technology Commission

Ministry of Science and Technology

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62475

Reference14 articles.

1. HEREDITARY PELLAGRA-LIKE SKIN RASH WITH TEMPORARY CEREBELLAR ATAXIA, CONSTANT RENAL AMINO-ACIDURIA, AND OTHER BIZARRE BIOCHEMICAL FEATURES

2. Novel Mutation in SLC6A19 Causing Late-Onset Seizures in Hartnup Disorder

3. Peripheral Neuropathy of the Alcoholic: I, Aetiological Role of Aneurin and Other B-complex Vitamins

4. Accurate discrimination of Hartnup disorder from other aminoacidurias using a diagnostic ratio

Cited by 6 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. Intestinal Amino Acid Transport and Metabolic Health;Annual Review of Nutrition;2023-08-21

2. Clinical Features and Laboratory Diagnosis of Aminoacidopathies: A Narrative Review;Archives of Neuroscience;2023-08-13

3. Hartnup disease;Radiopaedia.org;2023-07-20

4. New aspects for the brain in Hartnup disease based on mining of high-resolution cellular mRNA expression data for SLC6A19;IBRO Neuroscience Reports;2023-06

5. The hereditary spastic paraplegias;Handbook of Clinical Neurology;2023

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