Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome (Q85851515)
Jump to navigation
Jump to search
scientific article published on 16 August 2013
Language | Label | Description | Also known as |
---|---|---|---|
English | Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome |
scientific article published on 16 August 2013 |
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