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1 Ergebnisse
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First Case Report of FOXN1 Haploinsufficiency in China and ..:
LI Wendao
;
GU Hao
;
WANG Wei
..
https://xhyxzz.pumch.cn/en/article/doi/10.12290/xhyxzz.2022-0040. , 2023
Link:
https://doi.org/10.12290/xhyxzz.2022-0040
RT Journal T1 <Title>First Case Report of FOXN1 Haploinsufficiency in China and Literature Review</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:c8fe8c1497db445895090e44dbc45a6e&Exemplar=1&LAN=DE A1 LI Wendao A1 GU Hao A1 WANG Wei A1 WU Runhui A1 SONG Hongmei PB Editorial Office of Medical Journal of Peking Union Medical College Hospital YR 2023 K1 foxn1 mutation K1 combined immunodeficiency K1 syndromic features K1 Medicine K1 R JF https://xhyxzz.pumch.cn/en/article/doi/10.12290/xhyxzz.2022-0040 LK http://dx.doi.org/https://doi.org/10.12290/xhyxzz.2022-0040 DO https://doi.org/10.12290/xhyxzz.2022-0040 SF ELIB - SuUB Bremen
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