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Erratum: Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–...

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Erratum: Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1038_ejhg_2016_168

Erratum: Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders

About this item

Full title

Erratum: Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders

Author / Creator

van de Warrenburg, Bart P , Schouten, Meyke I , de Bot, Susanne T , Vermeer, Sascha , Meijer, Rowdy , Pennings, Maartje , Gilissen, Christian , Willemsen, Michèl AAP , Scheffer, Hans and Kamsteeg, Erik-Jan

Journal title

European journal of human genetics : EJHG, 2017-02, Vol.25 (3), p.393

Language

English

Formats

Articles

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Alternative Titles

Full title

Erratum: Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders

Authors, Artists and Contributors

Author / Creator

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_crossref_primary_10_1038_ejhg_2016_168

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1038_ejhg_2016_168

Other Identifiers

ISSN

1018-4813

E-ISSN

1476-5438

DOI

10.1038/ejhg.2016.168

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