Skip to main content
NCBI home page
Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2023 Jul 17;18:190. doi: 10.1186/s13023-023-02794-3

Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

Ali Zare Dehnavi 1, Maryam Bemanalizadeh 1,2, Seyyed Mohammad Kahani 3, Mahmoud Reza Ashrafi 1, Mohammad Rohani 4,5, Mehran Beiraghi Toosi 6,7, Morteza Heidari 1, Sareh Hosseinpour 1, Behnam Amini 1, Shaghayegh Zokaei 8,9, Zahra Rezaei 1, Hajar Aryan 8,10, Man Amanat 11, Hassan Vahidnezhad 12,13, Pouria Mohammadi 3,14, Masoud Garshasbi 3,✉, Ali Reza Tavasoli 1,12,14,✉
PMCID: PMC10353235  PMID: 37461050

Correction : Orphanet Journal of Rare Diseases (2023) 18:177 10.1186/s13023-023-02780-9

Following publication of the original article [1], we have been notified that the sentence on equal contribution of the first authors was missed. It should be as follows:

Ali Zare Dehanavi and Maryam Bemanalizadeh have contributed equally to this work.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Masoud Garshasbi, Email: Masoud.garshasbi@modares.ac.ir.

Ali Reza Tavasoli, Email: alirezatavasoli236@gmail.com.

Articles from Orphanet Journal of Rare Diseases are provided here courtesy of BMC

RESOURCES