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Distribution of ferritin complex in the adult brain and altered composition in neuroferritinopathy due to a novel variant in the ferritin heavy chain gene FTH1 (c.409_410del; p.H137Lfs4)
by
Ven, Peter F. M.
, Becker, Christina
, Ritschel, Nadja
, Alexopoulos, Ioannis
, Nishimura, Anna
, Weber, Axel
, Amsel, Daniel
, Schaiter, Alexander
, Roth, Angela
, Günther, Andreas
, Acker, Till
, Schänzer, Anne
, Selignow, Carmen
, Umathum, Vincent
, Németh, Attila
in
Amino acids
/ Brain
/ Cytoplasm
/ Disease
/ Ferritin
/ Genes
/ Morphology
/ Proteins
/ Research Letter
/ Research Letters
2024
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Distribution of ferritin complex in the adult brain and altered composition in neuroferritinopathy due to a novel variant in the ferritin heavy chain gene FTH1 (c.409_410del; p.H137Lfs4)
by
Ven, Peter F. M.
, Becker, Christina
, Ritschel, Nadja
, Alexopoulos, Ioannis
, Nishimura, Anna
, Weber, Axel
, Amsel, Daniel
, Schaiter, Alexander
, Roth, Angela
, Günther, Andreas
, Acker, Till
, Schänzer, Anne
, Selignow, Carmen
, Umathum, Vincent
, Németh, Attila
in
Amino acids
/ Brain
/ Cytoplasm
/ Disease
/ Ferritin
/ Genes
/ Morphology
/ Proteins
/ Research Letter
/ Research Letters
2024
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Distribution of ferritin complex in the adult brain and altered composition in neuroferritinopathy due to a novel variant in the ferritin heavy chain gene FTH1 (c.409_410del; p.H137Lfs4)
by
Ven, Peter F. M.
, Becker, Christina
, Ritschel, Nadja
, Alexopoulos, Ioannis
, Nishimura, Anna
, Weber, Axel
, Amsel, Daniel
, Schaiter, Alexander
, Roth, Angela
, Günther, Andreas
, Acker, Till
, Schänzer, Anne
, Selignow, Carmen
, Umathum, Vincent
, Németh, Attila
in
Amino acids
/ Brain
/ Cytoplasm
/ Disease
/ Ferritin
/ Genes
/ Morphology
/ Proteins
/ Research Letter
/ Research Letters
2024
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Distribution of ferritin complex in the adult brain and altered composition in neuroferritinopathy due to a novel variant in the ferritin heavy chain gene FTH1 (c.409_410del; p.H137Lfs4)
Journal Article
Distribution of ferritin complex in the adult brain and altered composition in neuroferritinopathy due to a novel variant in the ferritin heavy chain gene FTH1 (c.409_410del; p.H137Lfs4)
2024
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