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Characterization of mutations causing CYP21A2 deficiency in..:
Prado, Mayara Jorgens
;
Singh, Shripriya
;
Braun, Rodrigo Ligabue
...
International journal of molecular sciences. Basel. Vol. 23, no. 1 (Jan. 2022), e296, 19 p.. , 2022
Link:
http://hdl.handle.net/10183/267104
RT Journal T1 <Title>Characterization of mutations causing CYP21A2 deficiency in brazilian and portuguese populations</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftunivfrgs:oai:www.lume.ufrgs.br:10183_267104&Exemplar=1&LAN=DE A1 Prado, Mayara Jorgens A1 Singh, Shripriya A1 Braun, Rodrigo Ligabue A1 Meneghetti, Bruna Valandro A1 Serrano, Thaiane Rispoli A1 Kopacek, Cristiane A1 Monteiro, Karina Mariante A1 Zaha, Arnaldo A1 Rossetti, Maria Lucia Rosa A1 Pandey, Amit V YR 2022 K1 Tumor-derived exosomes K1 21-hydroxylase deficiency K1 Functional characterization K1 Hiperplasia adrenal congênita JF International journal of molecular sciences. Basel. Vol. 23, no. 1 (Jan. 2022), e296, 19 p. LK http://hdl.handle.net/10183/267104 DO http://hdl.handle.net/10183/267104 SF ELIB - SuUB Bremen
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