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

Ineke Labrijn-Marks, Galhana M. Somers-Bolman, Stijn L.M. In ’t Groen, Marianne Hoogeveen-Westerveld, Marian A. Kroos, Sirpa Ala-Mello, Olga Amaral, Clara sa Miranda, Irene Mavridou, Helen Michelakakis, Karin Naess, Frans W. Verheijen, Lies H. Hoefsloot, Trijnie Dijkhuizen, Marloes Benjamins, Hannerieke J.M. van den Hout, Ans T. van der Ploeg, W. W.M.Pim Pijnappel, Jasper J. Saris, Dicky J. Halley*

*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

10 Citations (Scopus)
17 Downloads (Pure)

Fingerprint

Dive into the research topics of 'Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays'. Together they form a unique fingerprint.

Biochemistry, Genetics and Molecular Biology