Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients
Más información
Título de la Revista: | Scientific Reports |
Volumen: | 7 |
Editorial: | Nature Publishing Group |
Fecha de publicación: | 2017 |
DOI/URL: |
10.1038/s41598-017-01896-w |