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1 Ergebnisse
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A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmen..:
Oe, Yuji
;
Mishima, Eikan
;
Mori, Takayasu
...
Internal Medicine. 60 (2021) 18 - p. 2991-2996 , 2021
Link:
https://doi.org/10.2169/internalmedicine.6987-20
RT Journal T1
A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype
UL https://suche.suub.uni-bremen.de/peid=cr-10.2169_internalmedicine.6987-20&Exemplar=1&LAN=DE A1 Oe, Yuji A1 Mishima, Eikan A1 Mori, Takayasu A1 Okamoto, Koji A1 Honkura, Yohei A1 Nagasawa, Tasuku A1 Yoshida, Mai A1 Sato, Hiroshi A1 Suzuki, Jun A1 Ikeda, Ryoukichi A1 Sohara, Eisei A1 Uchida, Shinichi A1 Katori, Yukio A1 Miyazaki, Mariko PB Japanese Society of Internal Medicine YR 2021 SN 0918-2918 SN 1349-7235 JF Internal Medicine VO 60 IS 18 SP 2991 OP 2996 LK http://dx.doi.org/https://doi.org/10.2169/internalmedicine.6987-20 DO https://doi.org/10.2169/internalmedicine.6987-20 SF ELIB - SuUB Bremen
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