A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

1. Ümraniye Training And Research Hospital, Clinic Of Pediatric Endocrinology, İstanbul, Turkey

2. King Abdulaziz University, Princess Al-Jawhara Albrahim Centre Of Excellence İn Research Of Hereditary Disorders, Jeddah, Saudi Arabia

3. St. George’S University Of London, Human Genetics Research Centre, Division Of Biomedical Sciences, London, United Kingdom

4. Quaid-I-Azam University Faculty Of Biological Sciences, Medical Genetics Research Laboratory, Department Of Biotechnology, Islamabad, Pakistan

5. Khyber Medical University, Institute Of Basic Medical Sciences, Department Of Biochemistry, Medical Genetics And Molecular Biology Unit, Peshawar, Pakistan