Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia

Research output: Contribution to journal › Letter › Contributed › peer-review

Contributors

Volker Endris - , Heidelberg University (Author)
Karl Hackmann - , Institute of Clinical Genetics (Author)
Teresa M. Neuhann - , Hereditary Cancer Syndrome Center (Author)
Ute Grasshoff - , University Hospital Tübingen (Author)
Michael Bonin - , University Hospital Tübingen (Author)
Ulrich Haug - , Clinic for Pediatric Neurology and Social Pediatrics Kinderzentrum Maulbronn gGmbH (Author)
Gabriele Hahn - , Department of Paediatrics (Author)
Jens C. Schallner - , Institute and Polyclinic of Diagnostic and Interventional Radiology (Author)
Evelin Schröck - , Institute of Clinical Genetics (Author)
Sigrid Tinschert - , Institute of Clinical Genetics (Author)
Gudrun Rappold - , Heidelberg University (Author)
Ute Moog - , Heidelberg University (Author)

Original language	English
Pages (from-to)	2908-2911
Number of pages	4
Journal	American Journal of Medical Genetics, Part A
Volume	152
Issue number	11
Publication status	Published - Nov 2010
Peer-reviewed	Yes

PubMed	20979196