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ACS Earth & Space Chemistry|February 18, 2020
Plutonium(IV) Sorption during Ferrihydrite Nanoparticle FormationKurt F Smith, Katherine Morris, Gareth T W Law, et al.
The Journal of Clinical Investigation|December 3, 2013
TTC7A mutations disrupt intestinal epithelial apicobasal polarityAmélie E Bigorgne, Henner F Farin, Roxane Lemoine, et al.
Molecular Genetics & Genomic Medicine|November 30, 2016
A potential founder variant in <i>CARMIL2/RLTPR</i> in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunctionHanne S Sorte, Liv T Osnes, Børre Fevang, et al.
Blood|January 3, 2001
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentationsA Villa, C Sobacchi, L D Notarangelo, et al.
Frontiers in Immunology|August 6, 2020
Second-Tier Next Generation Sequencing Integrated in Nationwide Newborn Screening Provides Rapid Molecular Diagnostics of Severe Combined ImmunodeficiencyJanne Strand, Kiran Aftab Gul, Hans Christian Erichsen, et al.
Immunology Today|November 1, 1996
CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndromeL D Notarangelo, M C Peitsch, T G Abrahamsen, et al.
American Journal of Human Genetics|June 17, 2014
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasiaAsbjørg Stray-Pedersen, Paul H Backe, Hanne S Sorte, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2016
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disordersAsbjørg Stray-Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon, et al.
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