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Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays

Crossref DOI link: https://doi.org/10.1038/s41431-019-0348-y

Published Online: 2019-02-08

Published Print: 2019-06

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Labrijn-Marks, Ineke

Somers-Bolman, Galhana M.

In ’t Groen, Stijn L. M.

Hoogeveen-Westerveld, Marianne

Kroos, Marian A.

Ala-Mello, Sirpa

Amaral, Olga

Miranda, Clara sa

Mavridou, Irene

Michelakakis, Helen

Naess, Karin

Verheijen, Frans W.

Hoefsloot, Lies H.

Dijkhuizen, Trijnie

Benjamins, Marloes

van den Hout, Hannerieke J. M.

van der Ploeg, Ans T.

Pijnappel, W. W. M. Pim

Saris, Jasper J. https://orcid.org/0000-0001-9232-267X
Halley, Dicky J.
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Text and Data Mining valid from 2019-02-08
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Article History

Received: 20 June 2018

Revised: 29 November 2018

Accepted: 8 January 2019

First Online: 8 February 2019

Compliance with ethical standards

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: The authors declare that they have no conflict of interest.