The p. Gly2019Ser is the commonest pathogenic mutation in the LRRK2 gene among Egyptians with familial and sporadic Parkinson's disease

Citation:
Salama, M., M. William, S. Hamed, A. Shalash, E. Khedr, M. Yousef, S. El-Jaafary, G. Fawi, A. Helmy, and E. Hamid, The p. Gly2019Ser is the commonest pathogenic mutation in the LRRK2 gene among Egyptians with familial and sporadic Parkinson's disease, , 2024.

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