Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1750-1172

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders ; volume:17 ; number:1 ; day:19 ; month:7 ; year:2022 ; pages:1-18 ; date:12.2022
Orphanet journal of rare diseases ; 17, Heft 1 (19.7.2022), 1-18, 12.2022

Creator: Borgia, Paola
Baldassari, Simona
Pedemonte, Nicoletta
Alkhunaizi, Ebba
D’Onofrio, Gianluca
Tortora, Domenico
Calì, Elisa
Scudieri, Paolo
Balagura, Ganna
Musante, Ilaria
Diana, Maria Cristina
Pedemonte, Marina
Vari, Maria Stella
Iacomino, Michele
Riva, Antonella
Chimenz, Roberto
Mangano, Giuseppe D.
Mohammadi, Mohammad Hasan
Toosi, Mehran Beiraghi
Ashrafzadeh, Farah
Imannezhad, Shima
Karimiani, Ehsan Ghayoor
Accogli, Andrea
Schiaffino, Maria Cristina
Maghnie, Mohamad
Soler, Miguel Angel
Echiverri, Karl
Abrams, Charles K.
Striano, Pasquale
Fortuna, Sara
Maroofian, Reza
Houlden, Henry
Zara, Federico
Fiorillo, Chiara
Salpietro, Vincenzo

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13023-022-02415-5

URN: urn:nbn:de:101:1-2022100120391405900415

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:32 AM CEST

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Associated

Borgia, Paola
Baldassari, Simona
Pedemonte, Nicoletta
Alkhunaizi, Ebba
D’Onofrio, Gianluca
Tortora, Domenico
Calì, Elisa
Scudieri, Paolo
Balagura, Ganna
Musante, Ilaria
Diana, Maria Cristina
Pedemonte, Marina
Vari, Maria Stella
Iacomino, Michele
Riva, Antonella
Chimenz, Roberto
Mangano, Giuseppe D.
Mohammadi, Mohammad Hasan
Toosi, Mehran Beiraghi
Ashrafzadeh, Farah
Imannezhad, Shima
Karimiani, Ehsan Ghayoor
Accogli, Andrea
Schiaffino, Maria Cristina
Maghnie, Mohamad
Soler, Miguel Angel
Echiverri, Karl
Abrams, Charles K.
Striano, Pasquale
Fortuna, Sara
Maroofian, Reza
Houlden, Henry
Zara, Federico
Fiorillo, Chiara
Salpietro, Vincenzo
SpringerLink (Online service)

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Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

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Other Objects (12)

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