Associated Papers
Exploring GBA1 gene in Parkinson's disease: Prevalence and variant spectrum from Asia minor.
Koç Yekedüz M et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2025
40542290 (PubMed )
Supplement: 10072_2025_8286_MOESM1_ESM.xlsx › T_M_HASTALAR
Novel deleterious mutation in MYO7A, TH and EVC2 in two Pakistani brothers with familial deafness.
Sabiha B et al.
Pakistan Journal of Medical Sciences, 0
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