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Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and..:
Kaustio, Meri
;
Nayebzadeh, Naemeh
;
Hinttala, Reetta
...
10.1016/j.jaci.2020.12.656. , 2021
Link:
http://hdl.handle.net/10138/335007
RT Journal T1
Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunction
UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_335007&Exemplar=1&LAN=DE A1 Kaustio, Meri A1 Nayebzadeh, Naemeh A1 Hinttala, Reetta A1 Tapiainen, Terhi A1 Astrom, Pirjo A1 Mamia, Katariina A1 Pernaa, Nora A1 Lehtonen, Johanna A1 Glumoff, Virpi A1 Rahikkala, Elisa A1 Honkila, Minna A1 Olsen, Paivi A1 Hassinen, Antti A1 Polso, Minttu A1 Al Sukaiti, Nashat A1 Al Shekaili, Jalila A1 Al Kindi, Mahmood A1 Al Hashmi, Nadia A1 Almusa, Henrikki A1 Bulanova, Daria A1 Haapaniemi, Emma A1 Chen, Pu A1 Suo-Palosaari, Maria A1 Vieira, Paivi A1 Tuominen, Hannu A1 Kokkonen, Hannaleena A1 Al Macki, Nabil A1 Al Habsi, Huda A1 Löppönen, Tuija A1 Rantala, Heikki A1 Pietiäinen, Vilja A1 Zhang, Shen-Ying A1 Renko, Marjo A1 Hautala, Timo A1 Al Farsi, Tariq A1 Uusimaa, Johanna A1 Saarela, Janna PB Mosby Elsevier YR 2021 K1 DIAPH1 K1 SCBMS K1 microcephaly K1 mitochondrial dysfunction K1 T cells K1 immunodeficiency K1 T-CELL-ACTIVATION K1 FORMIN K1 MDIA1 K1 POLARIZATION K1 MUTATIONS K1 MIGRATION K1 HOMOLOG K1 PROTEIN K1 ROCK K1 RHOA K1 1182 Biochemistry K1 cell and molecular biology JF 10.1016/j.jaci.2020.12.656 LK http://hdl.handle.net/10138/335007 DO http://hdl.handle.net/10138/335007 SF ELIB - SuUB Bremen
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