Published in
Elsevier, European Journal of Medical Genetics, 10(59), p. 549-553
DOI: 10.1016/j.ejmg.2016.09.002
Links
Tools
Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1
Journal article published in 2016 by
Bernt Popp 
,
Regina Trollmann,
Christian Büttner,
Almuth Caliebe,
Christian T. Thiel,
Ulrike Hüffmeier,
André Reis ,
Christiane Zweier
,
Regina Trollmann,
Christian Büttner,
Almuth Caliebe,
Christian T. Thiel,
Ulrike Hüffmeier,
André Reis ,
Christiane Zweier
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 