Betül Okur Altındaş

2PUBLICATIONS
6CO-AUTHORS
Gene mappingCancer genetics
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Publications (2)

|Aug 09, 2025
Uncovering the CLCN1 Y150* nonsense variant in myotonia congenita: genetic evidence from segregation analysis.

Betül Okur Altındaş, Ayse Gul Zamani, Figen Güney

|Jul 03, 2025
Clinical Vigilance in Rare Disease Management: Atypical Features Lead to Discovery of Concurrent X-linked Adrenoleukodystrophy and Cystic Fibrosis.

Kübra Taşar Ünsaçar, Betül Okur Altındaş, Hüseyin Çaksen

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Frequent Collaborators

2 joint publications

Ayşe Gül Zamani

1 joint publications

Kübra Taşar Ünsaçar

1 joint publications

Hüseyin Çaksen

1 joint publications

Sevgi Pekcan