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1 Ergebnisse
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Fatal congenital copper transport defect caused by a homozy..:
Dame, Christof
;
Horn, Denise
;
Schomburg, Lutz
...
Clinical Genetics. 103 (2022) 5 - p. 585-589 , 2022
Link:
https://doi.org/10.1111/cge.14289
RT Journal T1
Fatal congenital copper transport defect caused by a homozygous likely pathogenic variant of SLC31A1
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14289&Exemplar=1&LAN=DE A1 Dame, Christof A1 Horn, Denise A1 Schomburg, Lutz A1 Grünhagen, Johannes A1 Chillon, Thilo Samson A1 Tietze, Anna A1 Vogt, Annika A1 Bührer, Christoph PB Wiley YR 2022 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 103 IS 5 SP 585 OP 589 LK http://dx.doi.org/https://doi.org/10.1111/cge.14289 DO https://doi.org/10.1111/cge.14289 SF ELIB - SuUB Bremen
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