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

Dehnavi AZ, Bemanalizadeh M, Kahani SM, Ashrafi MR, Rohani M, Toosi MB, Heidari M, Hosseinpour S, Amini B, Zokaei S, Rezaei Z, Aryan H, Amanat M, Vahidnezhad H, Mohammadi P, Garshasbi M, Tavasoli AR

Open source

DOI
10.1186/s13023-023-02780-9
Published
2023 Jul 5
Container
Orphanet journal of rare diseases
Publisher
Not recorded
Open access
yes

Credibility signals

limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

Cite this work

BibTeX

@article{allodium:10.1186/s13023-023-02780-9,
  title = {Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.},
  author = {Dehnavi AZ and Bemanalizadeh M and Kahani SM and Ashrafi MR and Rohani M and Toosi MB and Heidari M and Hosseinpour S and Amini B and Zokaei S and Rezaei Z and Aryan H and Amanat M and Vahidnezhad H and Mohammadi P and Garshasbi M and Tavasoli AR},
  year = {2023},
  journal = {Orphanet journal of rare diseases},
  doi = {10.1186/s13023-023-02780-9},
  url = {https://doi.org/10.1186/s13023-023-02780-9}
}

RIS

TY  - JOUR
TI  - Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.
AU  - Dehnavi AZ
AU  - Bemanalizadeh M
AU  - Kahani SM
AU  - Ashrafi MR
AU  - Rohani M
AU  - Toosi MB
AU  - Heidari M
AU  - Hosseinpour S
AU  - Amini B
AU  - Zokaei S
AU  - Rezaei Z
AU  - Aryan H
AU  - Amanat M
AU  - Vahidnezhad H
AU  - Mohammadi P
AU  - Garshasbi M
AU  - Tavasoli AR
PY  - 2023
JO  - Orphanet journal of rare diseases
DO  - 10.1186/s13023-023-02780-9
UR  - https://doi.org/10.1186/s13023-023-02780-9
ER  - 

APA

AZ, D., M, B., SM, K., MR, A., M, R., MB, T., M, H., S, H., B, A., S, Z., Z, R., H, A., M, A., H, V., P, M., M, G., & AR, T. (2023). Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-023-02780-9

Source records