Login / Signup
Mehmet Bugrahan Duz
ORCID
Publication Activity (10 Years)
Years Active: 2021-2021
Publications (10 Years): 2
Top Topics
High Throughput Sequencing
Temporal Lobe Epilepsy
Chronic Kidney Disease
Late Onset
Top Venues
Neurocase
Global medical genetics
</>
This page only lists publications with an associated author ORCID identifier.
Publications
</>
Mehmet Bugrahan Duz
A novel CLN5 mutation in Turkish patient with variant late-onset neuronal ceroid lipofuscinosis and recurrent fractures that causes severe morbidity.
Neurocase
(2021)
Aysel Kalaycı Yiğin
,
Mehmet Bugrahan Duz
,
Mehmet Seven
Rare Findings in Cleidocranial Dysplasia Caused by RUNX Mutation.
Global medical genetics
9 (1) (2021)