Publications:

A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP.

Journal Of Human Genetics

Çağlayan, Ahmet O AO; Tüysüz, Beyhan B; Coşkun, Süleyman S; Quon, Jennifer J; Harmancı, Akdes S AS; Baranoski, Jacob F JF; Baran, Burçin B; Erson-Omay, E Zeynep EZ; Henegariu, Octavian O; Mane, Shrikant M SM; Bilgüvar, Kaya K; Yasuno, Katsuhito K; Günel, Murat M

Publication Date: 2016-05

Variant appearance in text: FTO: 1207C>T

PubMed Link: 26740239

Variant Present in the following documents:

• Main text
• nihms742086.pdf

View BVdb publication page