Publications

Segmental and Total Uniparental Isodisomy (Upid) as a Disease Mechanism in Autosomal Recessive Lysosomal Disorders: Evidence from Snp Arrays

AuthID
P-00Q-7GM

Author(s)

Labrijn Marks, I

Somers Bolman, GM

Groen, SLMI

Hoogeveen Westerveld, M

Kroos, MA

Amaral, O

Mavridou, I

Naess, K

Hoefsloot, LH

Dijkhuizen, T

Benjamins, M

van den Hout, HJM

van der Ploeg, AT

Pijnappel, WWMP

Saris, JJ

Halley, DJ

Document Type

Article

Year published

2019

Published

in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813

Volume: 27, Issue: 6, Pages: 919-927 (9)

Indexing

Wos^®

Scopus^®

Google Scholar^®

Metadata
Sources

Publication Identifiers

DOI: 10.1038/s41431-019-0348-y

Scopus: 2-s2.0-85061283350

Wos: WOS:000467381900010

Source Identifiers

ISSN: 1018-4813

Export Publication Metadata

Marked List

Add to Marked List

Info

At this moment we don't have any links to full text documens.

Segmental and Total Uniparental Isodisomy (Upid) as a Disease Mechanism in Autosomal Recessive Lysosomal Disorders: Evidence from Snp Arrays

Useful Links

Get Help

Federated Authentication (Click on the image)

Segmental and Total Uniparental Isodisomy (Upid) as a Disease Mechanism in Autosomal Recessive Lysosomal Disorders: Evidence from Snp Arrays

Useful Links

Get Help