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Enes Gündüz
ORCID
Publication Activity (10 Years)
Years Active: 2024-2024
Publications (10 Years): 6
Top Topics
Genome Wide Analysis
Autism Spectrum Disorder
Prognostic Factors
Patient Reported Outcomes
Top Venues
Orphanet journal of rare diseases
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This page only lists publications with an associated author ORCID identifier.
Publications
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Muhammed Köroglu
,
Mustafa Karakaplan
,
Enes Gündüz
,
Betül Kesriklioğlu
,
Emre Ergen
,
Okan Aslantürk
,
Zeynep Maraş Özdemir
Cerebrotendinous Xanthomatosis patients with late diagnosed in single orthopedic clinic: two novel variants in the CYP27A1 gene.
Orphanet journal of rare diseases
19 (1) (2024)
Muhammed Köroglu
,
Mustafa Karakaplan
,
Enes Gündüz
,
Betül Kesriklioğlu
,
Emre Ergen
,
Okan Aslantürk
,
Zeynep Maraş Özdemir
Cerebrotendinous Xanthomatosis patients with late diagnosed in single orthopedic clinic: two novel variants in the CYP27A1 gene.
Orphanet journal of rare diseases
19 (1) (2024)
Muhammed Köroglu
,
Mustafa Karakaplan
,
Enes Gündüz
,
Betül Kesriklioğlu
,
Emre Ergen
,
Okan Aslantürk
,
Zeynep Maraş Özdemir
Cerebrotendinous Xanthomatosis patients with late diagnosed in single orthopedic clinic: two novel variants in the CYP27A1 gene.
Orphanet journal of rare diseases
19 (1) (2024)
Muhammed Köroglu
,
Mustafa Karakaplan
,
Enes Gündüz
,
Betül Kesriklioğlu
,
Emre Ergen
,
Okan Aslantürk
,
Zeynep Maraş Özdemir
Cerebrotendinous Xanthomatosis patients with late diagnosed in single orthopedic clinic: two novel variants in the CYP27A1 gene.
Orphanet journal of rare diseases
19 (1) (2024)
Muhammed Köroglu
,
Mustafa Karakaplan
,
Enes Gündüz
,
Betül Kesriklioğlu
,
Emre Ergen
,
Okan Aslantürk
,
Zeynep Maraş Özdemir
Cerebrotendinous Xanthomatosis patients with late diagnosed in single orthopedic clinic: two novel variants in the CYP27A1 gene.
Orphanet journal of rare diseases
19 (1) (2024)
Muhammed Köroglu
,
Mustafa Karakaplan
,
Enes Gündüz
,
Betül Kesriklioğlu
,
Emre Ergen
,
Okan Aslantürk
,
Zeynep Maraş Özdemir
Cerebrotendinous Xanthomatosis patients with late diagnosed in single orthopedic clinic: two novel variants in the CYP27A1 gene.
Orphanet journal of rare diseases
19 (1) (2024)