The first Turkish family with Rotor syndrome diagnosed at the molecular level

por Gümüş, Evren, Karaca, Meryem, Deveci, Uğur, Jirsa, Milan
Publicado 2020

Triosephosphate Isomerase Deficiency: E105D Mutation in Unrelated Patients and Review of the Literature

por Selamioğlu, Arzu, Karaca, Meryem, Balcı, Mehmet Cihan, Körbeyli, Hüseyin Kutay, Durmuş, Aslı, Yıldız, Edibe Pembegül, Karaman, Serap, Gökçay, Gülden Fatma
Publicado 2023

Clinical and bi-genomic DNA findings of patients suspected to have mitochondrial diseases

por Gedikbasi, Asuman, Toksoy, Guven, Karaca, Meryem, Gulec, Cagri, Balci, Mehmet Cihan, Gunes, Dilek, Gunes, Seda, Aslanger, Ayca Dilruba, Unverengil, Gokcen, Karaman, Birsen, Basaran, Seher, Demirkol, Mubeccel, Gokcay, Gulden Fatma, Uyguner, Zehra Oya
Publicado 2023