Mutluay Arslan

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 3

Top Topics

Intellectual Disability

Top Venues

American journal of medical genetics. Part A

Journal of clinical research in pediatric endocrinology

This page only lists publications with an associated author ORCID identifier.

Publications

Sara Capiau, Joél Smet, Boel De Paepe, Yilmaz Yildiz, Mutluay Arslan, Olivier Stevens, Maxime Verschoore, Hedwig Stepman, Sara Seneca, Arnaud Vanlander
Clinical Heterogeneity in MT-ATP6 Pathogenic Variants: Same Genotype-Different Onset. Cells 11 (3) (2022)
Deniz Torun, Mutluay Arslan, Zafer Yüksel
Coexistence of severe developmental delay, epilepsy, and hemangioma in Snijders Blok-Fisher syndrome suggests the presence of a POU3F3-related SNIBFIS endophenotype: A case report. American journal of medical genetics. Part A 185 (5) (2021)
Mina Mısırlıgil, Yilmaz Yildiz, Onur Akın, Sevinç Odabaşı Güneş, Mutluay Arslan, Bülent Unay
A Rare Cause of Hyperinsulinemic Hypoglycemia: Kabuki Syndrome Journal of clinical research in pediatric endocrinology 13 (4) (2020)