Advanced search
Publication Cover
International Journal of Neuroscience Volume 131, 2021 - Issue 10
Submit an article Journal homepage
229
Views
7
CrossRef citations to date
0
Altmetric
Original Articles

CAPN1 and hereditary spastic paraplegia: a novel variant in an Iranian family and overview of the genotype-phenotype correlation

Mohammad Masoud Rahimi Bidgolia Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, IranView further author information
,
Leila Javanparasta Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, IranView further author information
,
Mohammad Rohanib Department of Neurology, Iran University of Medical Sciences, Hazrat Rasool Hospital, Tehran, IranView further author information
,
Hossein Najmabadia Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, IranView further author information
,
Babak Zamanic Neurology Department, Firoozgar Hospital, Iran University of Medical Sciences, Tehran, IranView further author information
&
Afagh Alavia Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, IranCorrespondence[email protected]
View further author information
Pages 962-974 | Received 03 Feb 2020, Accepted 17 Apr 2020, Published online: 13 May 2020

Citations (7)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (1)

Mahdieh Pashaei, Atefeh Davarzani, Reza Hajati, Babak Zamani, Shahriar Nafissi, Farzaneh Larti, Yalda Nilipour, Mohammad Rohani & Afagh Alavi. (2021) Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families. Journal of Neurogenetics 35:2, pages 84-94.
Read now

Articles from other publishers (6)

Abdulrahman Alkhalifa, Shihan Chen, Zehra Isik Hasiloglu, Massimiliano Filosto, Elisa Cali, Henry Houlden, Paulo Sgobbi de Souza, Afagh Alavi, Cyril Goizet, Giovanni Stevanin, Frederic Taithe, Francesco Nicita, Gessica Vasco, Stefano Tozza, Sirio Cocozza, Nicola Carboni, Andrea Figus, Jianjun Wu, A. Nazli Basak, Bernard Brais, Guy Rouleau & Roberta La Piana. (2023) White matter abnormalities in 15 subjects with SPG76. Journal of Neurology 270:12, pages 5784-5792.
Crossref
Zeyu Zhu, Wenzhe Hou, Yuwen Cao, Haoran Zheng, Wotu Tian & Li Cao. (2023) Spastic paraplegia type 76 due to novel CAPN1 mutations: three case reports with literature review. neurogenetics.
Crossref
Aida Ghasemi, Zahra Sadr, Mojgan Babanejad, Mohammad Rohani & Afagh Alavi. (2023) Copy Number Variations in Hereditary Spastic Paraplegia-Related Genes: Evaluation of an Iranian Hereditary Spastic Paraplegia Cohort and Literature Review. Molecular Syndromology 14:6, pages 477-484.
Crossref
Ayush Agarwal, Rahul Oinam, Vinay Goel, Pooja Sharma, Mohd. Faruq, Ajay Garg & Achal K. Srivastava. (2022) “Ear of the Lynx” Sign in Hereditary Spastic Paraparesis ( HSP ) 76 . Movement Disorders Clinical Practice 10:1, pages 120-123.
Crossref
Jean-Loup Méreaux, Cristina Firanescu, Giulia Coarelli, Malin Kvarnung, Rita Rodrigues, Elena Pegoraro, Meriem Tazir, Frédéric Taithe, Rémi Valter, Vincent Huin, Kristina Lidström, Guillaume Banneau, Sara Morais, Livia Parodi, Marie Coutelier, Mélanie Papin, Per Svenningsson, Jean-Philippe Azulay, Isabel Alonso, Daniel Nilsson, Alexis Brice, Eric Le Guern, Rayomand Press, Giovanni Vazza, José Leal Loureiro, Cyril Goizet, Alexandra Durr, Martin Paucar & Giovanni Stevanin. (2021) Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations. neurogenetics 22:1, pages 71-79.
Crossref
Lu‐Lu Lai, Yi‐Jun Chen, Yun‐Lu Li, Xiao‐Hong Lin, Meng‐Wen Wang, En‐Lin Dong, Ning Wang, Wan‐Jin Chen & Xiang Lin. (2020) Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia . Annals of Clinical and Translational Neurology 7:10, pages 1862-1869.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.