(Q85851515)
Statements
Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome (English)
Sheila Unger
Andrea Superti-Furga
Luisa Bonafé
Belinda Campos-Xavier
Esra Dikoglu
Pelin Ozlem Simsek-Kiper
Gulen Eda Utine
Koray Boduroglu