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Author/Creator van Alphen, Floris

1. A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia. (4th March 2019)

Authors:
Klei, Thomas R. L.; Kheradmand Kia, Sima; Veldthuis, Martijn; Dehbozorgian, Javad; Karimi, Mehran; Geissler, Judy; Sellink, Erica; Thiel-Valkhof, Marijke; Burger, Patrick; van Alphen, Floris; Meijer, Alexander B.; van Bruggen, Robin; van Zwieten, Rob
Journal:
Hemoglobin
Issue:
Volume 43:Number 2(2019)
Page Start:
77
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Hermansky–Pudlak syndrome type 2: Aberrant pre‐mRNA splicing and mislocalization of granule proteins in neutrophils. Issue 10 (15th June 2017)

Authors:
de Boer, Martin; van Leeuwen, Karin; Geissler, Judy; van Alphen, Floris; de Vries, Esther; van der Kuip, Martijn; Terheggen, Suzanne W.J.; Janssen, Hans; van den Berg, Timo K.; Meijer, Alexander B.; Roos, Dirk; Kuijpers, Taco W.
Journal:
Human mutation
Issue:
Volume 38:Issue 10(2017)
Page Start:
1402
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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