Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene-disease associations and unanticipated rare disorders
Eur J Hum Genet
.
2017 Feb;25(3):393.
doi: 10.1038/ejhg.2016.168.
Authors
Bart P van de Warrenburg
,
Meyke I Schouten
,
Susanne T de Bot
,
Sascha Vermeer
,
Rowdy Meijer
,
Maartje Pennings
,
Christian Gilissen
,
Michèl Aap Willemsen
,
Hans Scheffer
,
Erik-Jan Kamsteeg
PMID:
28179632
PMCID:
PMC5315505
DOI:
10.1038/ejhg.2016.168
No abstract available
Publication types
Published Erratum