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Yenan T. Bryceson
Yenan T. Bryceson
Epilepsy
Hypotonia
Genetics
Missense mutation
Biology
3
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36
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First report of an SH2D1A mutation associated with X-linked lymphoproliferative disease in Turkey
2018
Turkish Journal of Hematology
Selman Kesici
Ebru Yilmaz-Keskin
Samuel C. C. Chiang
Çiğdem Seher Kasapkara
Takuya Sekine
Meltem Akcaboy
Ali Fettah
Yenan T. Bryceson
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Citations (1)
Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype
2016
Genes
Nadia Skauli
Sean Wallace
Samuel C. C. Chiang
Tuva Barøy
Asbjørn Holmgren
Asbjørg Stray-Pedersen
Yenan T. Bryceson
Petter Strømme
Eirik Frengen
Doriana Misceo
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Citations (19)
Site-Specific Photolabeling of the IgG Fab Fragment Using a Small Protein G Derived Domain
2016
Bioconjugate Chemistry
Sara Kanje
Emma von Witting
Samuel C. C. Chiang
Yenan T. Bryceson
Sophia Hober
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Citations (16)
1