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CYB5R3 homozygous pathogenic variant as a rare cause of cya..:
Molina Herranz, D.
;
García Escudero, C.
;
Rite Gracia, S.
...
Clinical Biochemistry. 102 (2022) - p. 67-70 , 2022
Link:
https://doi.org/10.1016/j.clinbiochem.2022.01.008
RT Journal T1
CYB5R3 homozygous pathogenic variant as a rare cause of cyanosis in the newborn
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.clinbiochem.2022.01.008&Exemplar=1&LAN=DE A1 Molina Herranz, D. A1 García Escudero, C. A1 Rite Gracia, S. A1 Aguilar de la Red, Y. A1 Martínez Nieto, J. A1 Izquierdo Álvarez, S. A1 Montañés Gracia, M.A. A1 Recasens, V. A1 Hernández Mata, C.F. PB Elsevier BV YR 2022 SN 0009-9120 JF Clinical Biochemistry VO 102 SP 67 OP 70 LK http://dx.doi.org/https://doi.org/10.1016/j.clinbiochem.2022.01.008 DO https://doi.org/10.1016/j.clinbiochem.2022.01.008 SF ELIB - SuUB Bremen
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