Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome
2012
Bert DeVries and colleagues identify mutations in the chromatin regulator KANSL1 in 17q21.31 microdeletion syndrome. This syndrome is characterized by intellectual disability, hypotonia and distinctive facial features.
Keywords:
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
14
References
158
Citations
NaN
KQI