Open AccessTwo male patients from an extended seven generation Turkish family diagnosed with Renpenning syndrome: identifying the causative mutation and review of the literature
Author(s) -
Bayram Toraman,
Tuba Dinçer,
Gülden Yorgancıoğlu Budak,
Çilem Bilginer,
Hülya Kayserili,
Ersan Kalay
Publication year - 2022
Publication title -
the european research journal
Language(s) - English
Resource type - Journals
ISSN - 2149-3189
DOI - 10.18621/eurj.924346
Subject(s) - medicine , proband , sanger sequencing , genetics , intellectual disability , exome sequencing , disease , mutation , gene , biology , psychiatry