المؤلفون: Seyedtaghia, M.R., Soudyab, M., Shariati, M., Esfehani, R.J., Vafadar, S., Shalaei, N., Nouri, V., Zech, M., Winkelmann, J., Shoeibi, A., Sadr-Nabavi, A.

المصدر: Heliyon 9:e15393 (2023)

مصطلحات موضوعية: Alu Repeats, Cnv, Park7, Parkinson's Disease, Wes

Relation: info:eu-repo/semantics/altIdentifier/pmid/37095917; info:eu-repo/semantics/altIdentifier/wos/000999721900001; info:eu-repo/semantics/altIdentifier/isbn/2405-8440; info:eu-repo/semantics/

الاتاحة: https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=67668
https://doi.org/10.1016/j.heliyon.2023.e15393

المؤلفون: Soudyab, M., Shariati, M., Esfehani, R.J., Shalaei, N., Vafadar, S., Nouri, V., Zech, M., Winkelmann, J., Shoeibi, A., Sadr-Nabavi, A.

المصدر: J. Mol. Neurosci. 72, 2486-2496 (2022)

مصطلحات موضوعية: Causative Variants, Genetics, Genotype, Parkinson’s Disease, Whole-exome Sequencing

Relation: info:eu-repo/semantics/altIdentifier/pmid/36520381; info:eu-repo/semantics/altIdentifier/wos/000899479500002; info:eu-repo/semantics/altIdentifier/isbn/0895-8696; info:eu-repo/semantics/alt

الاتاحة: https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=66982
https://doi.org/10.1007/s12031-022-02085-9