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Genotype–phenotype correlations and disease mechanisms in P..:
Borgia, Paola
;
Baldassari, Simona
;
Pedemonte, Nicoletta
...
Orphanet Journal of Rare Diseases. 17 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/s13023-022-02415-5
RT Journal T1
Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s13023-022-02415-5&Exemplar=1&LAN=DE A1 Borgia, Paola A1 Baldassari, Simona A1 Pedemonte, Nicoletta A1 Alkhunaizi, Ebba A1 D'Onofrio, Gianluca A1 Tortora, Domenico A1 Calì, Elisa A1 Scudieri, Paolo A1 Balagura, Ganna A1 Musante, Ilaria A1 Diana, Maria Cristina A1 Pedemonte, Marina A1 Vari, Maria Stella A1 Iacomino, Michele A1 Riva, Antonella A1 Chimenz, Roberto A1 Mangano, Giuseppe D. A1 Mohammadi, Mohammad Hasan A1 Toosi, Mehran Beiraghi A1 Ashrafzadeh, Farah A1 Imannezhad, Shima A1 Karimiani, Ehsan Ghayoor A1 Accogli, Andrea A1 Schiaffino, Maria Cristina A1 Maghnie, Mohamad A1 Soler, Miguel Angel A1 Echiverri, Karl A1 Abrams, Charles K. A1 Striano, Pasquale A1 Fortuna, Sara PB Springer Science and Business Media LLC YR 2022 SN 1750-1172 JF Orphanet Journal of Rare Diseases VO 17 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s13023-022-02415-5 DO https://doi.org/10.1186/s13023-022-02415-5 SF ELIB - SuUB Bremen
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