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Variation of the clinical spectrum and genotype-phenotype a..:

Drovandi, Stefania ; Lipska-Ziętkiewicz, Beata S ; Ozaltin, Fatih...
Drovandi, Stefania Lipska-Ziętkiewicz, Beata S. Ozaltin, Fatih Emma, Francesco Gulhan, Bora Boyer, Olivia Trautmann, Agnes Ziętkiewicz, Szymon Xu, Hong Shen, Qian Rao, Jia Riedhammer, Korbinian M. Heemann, Uwe Hoefele, Julia Stenton, Sarah L. Tsygin, Alexey N. Ng, Kar-Hui Fomina, Svitlana Benetti, Elisa Aurelle, Manon Prikhodina, Larisa Schijvens, Anne M. Tabatabaeifar, Mansoureh Jankowski, Maciej Baiko, Sergey Mao, Jianhua Feng, Chunyue Deng, Fang Rousset-Rouviere, Caroline Stańczyk, Małgorzata Bałasz-Chmielewska, Irena Fila, Marc Durkan, Anne M. Levart, Tanja Kersnik Dursun, Ismail Esfandiar, Nasrin Haas, Dorothea Bjerre, Anna Kristina Anarat, Ali Benz, Marcus R. Talebi, Saeed Hooman, Nakysa Ariceta, Gema Schaefer, Franz . Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy. Kidney International. 2022, 102(3), 592-603. , 2022

Link: http://hdl.handle.net/10852/99032

RT Journal
T1 <Title>Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy ; ENEngelskEnglishVariation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftoslouniv:oai:www.duo.uio.no:10852_99032&Exemplar=1&LAN=DE
				
A1 Drovandi, Stefania
A1 Lipska-Ziętkiewicz, Beata S
A1 Ozaltin, Fatih
A1 Emma, Francesco
A1 Gulhan, Bora
A1 Boyer, Olivia
A1 Trautmann, Agnes
A1 Ziętkiewicz, Szymon
A1 Xu, Hong
A1 Shen, Qian
A1 Rao, Jia
A1 Riedhammer, Korbinian M
A1 Heemann, Uwe
A1 Hoefele, Julia
A1 Stenton, Sarah L
A1 Tsygin, Alexey N
A1 Ng, Kar-Hui
A1 Fomina, Svitlana
A1 Benetti, Elisa
A1 Aurelle, Manon
A1 Prikhodina, Larisa
A1 Schijvens, Anne M
A1 Tabatabaeifar, Mansoureh
A1 Jankowski, Maciej
A1 Baiko, Sergey
A1 Mao, Jianhua
A1 Feng, Chunyue
A1 Deng, Fang
A1 Rousset-Rouviere, Caroline
A1 Stańczyk, Małgorzata
A1 Bałasz-Chmielewska, Irena
A1 Fila, Marc
A1 Durkan, Anne M
A1 Levart, Tanja Kersnik
A1 Dursun, Ismail
A1 Esfandiar, Nasrin
A1 Haas, Dorothea
A1 Bjerre, Anna Kristina
A1 Anarat, Ali
A1 Benz, Marcus R
A1 Talebi, Saeed
A1 Hooman, Nakysa
A1 Ariceta, Gema
A1 Schaefer, Franz
YR 2022
JF Drovandi, Stefania Lipska-Ziętkiewicz, Beata S. Ozaltin, Fatih Emma, Francesco Gulhan, Bora Boyer, Olivia Trautmann, Agnes Ziętkiewicz, Szymon Xu, Hong Shen, Qian Rao, Jia Riedhammer, Korbinian M. Heemann, Uwe Hoefele, Julia Stenton, Sarah L. Tsygin, Alexey N. Ng, Kar-Hui Fomina, Svitlana Benetti, Elisa Aurelle, Manon Prikhodina, Larisa Schijvens, Anne M. Tabatabaeifar, Mansoureh Jankowski, Maciej Baiko, Sergey Mao, Jianhua Feng, Chunyue Deng, Fang Rousset-Rouviere, Caroline Stańczyk, Małgorzata Bałasz-Chmielewska, Irena Fila, Marc Durkan, Anne M. Levart, Tanja Kersnik Dursun, Ismail Esfandiar, Nasrin Haas, Dorothea Bjerre, Anna Kristina Anarat, Ali Benz, Marcus R. Talebi, Saeed Hooman, Nakysa Ariceta, Gema Schaefer, Franz . Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy. Kidney International. 2022, 102(3), 592-603
LK http://hdl.handle.net/10852/99032
DO http://hdl.handle.net/10852/99032
SF ELIB - SuUB Bremen

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