Aydan Değerliyurt

3PUBLICATIONS
15CO-AUTHORS
Neurology and neuromuscular diseasesPeripheral nervous systemMedical biochemistry - inorganic elements and compounds
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Publications (3)

|Jul 19, 2026
Genotypic and phenotypic heterogeneity in tubulinopathies: insights from a Turkish multicenter cohort.

|Jun 27, 2022
Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene.

Aydan Değerliyurt, Nadide Başak Gülleroğlu, Ayşe Esin Kibar Gül

|Aug 16, 2021
Significant neuropsychiatric symptoms: three mucopolysaccharidosis type IIIB cases, two of whom were siblings with a novel NAGLU gene mutation.

Aydan Değerliyurt, Özlem Yayıcı Köken, Neslihan Düzkale Teker

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Frequent Collaborators

1 joint publications

Özlem Yayıcı Köken

1 joint publications

Neslihan Düzkale Teker

1 joint publications

Dilek Aktaş

1 joint publications

Nadide Başak Gülleroğlu