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1 Ergebnisse
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A null founder variant in NPNT, encoding nephronectin, caus..:
Al‐Hamed, Mohamed H.
;
Altuwaijri, Norah
;
Alsahan, Nada
...
Clinical Genetics. 102 (2022) 1 - p. 61-65 , 2022
Link:
https://doi.org/10.1111/cge.14128
RT Journal T1
A null founder variant in NPNT, encoding nephronectin, causes autosomal recessive renal agenesis
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14128&Exemplar=1&LAN=DE A1 Al‐Hamed, Mohamed H. A1 Altuwaijri, Norah A1 Alsahan, Nada A1 Ali, Wafaa A1 Abdulwahab, Firdous A1 Alzahrani, Fatema A1 Majrashi, Nada A1 Alkuraya, Fowzan S. PB Wiley YR 2022 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 102 IS 1 SP 61 OP 65 LK http://dx.doi.org/https://doi.org/10.1111/cge.14128 DO https://doi.org/10.1111/cge.14128 SF ELIB - SuUB Bremen
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