دورية أكاديمية
Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays
| العنوان: | Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays |
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| المؤلفون: | Labrijn-Marks, Ineke, Somers-Bolman, Galhana M., In ’t Groen, Stijn L. M.Aff2, Aff3, Aff4, Hoogeveen-Westerveld, MarianneAff1, Aff2, Aff4, Kroos, Marian A.Aff1, Aff2, Aff4, 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.Aff3, Aff4, van der Ploeg, Ans T.Aff3, Aff4, Pijnappel, W. W. M. PimAff2, Aff3, Aff4, Saris, Jasper J., Halley, Dicky J.Aff1 |
| المصدر: | European Journal of Human Genetics. 27(6):919-927 |
| قاعدة البيانات: | Springer Nature Journals |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 10184813 14765438 |
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| DOI: | 10.1038/s41431-019-0348-y |