Genotype-Phenotype Correlations and Disease Mechanisms in Pex13-Related Zellweger Spectrum Disorders

AuthID
P-015-J7Z
35
Author(s)
Borgia, P
·
Baldassari, S
·
Pedemonte, N
·
Alkhunaizi, E
·
D'Onofrio, G
·
Tortora, D
·
Calì, E
·
Scudieri, P
·
Balagura, G
·
Musante, I
·
[+15]·
Echiverri, K
·
Abrams, CK
·
Striano, P
·
Fortuna, S
·
Maroofian, R
·
Houlden, H
·
Zara, F
·
Fiorillo, C
·
Salpietro, V
Document Type
Article
Year published
2022
Published
in ORPHANET JOURNAL OF RARE DISEASES
Volume: 17, Issue: 1
Indexing
Publication Identifiers
Pubmed: 35854306
Scopus: 2-s2.0-85134372879
Wos: WOS:000827764600005
Export Publication Metadata
Marked List
Info
At this moment we don't have any links to full text documens.
Name Order Name   Name Order Name   Name Order Name
1 Borgia, P;   2 Baldassari, S;   3 Pedemonte, N;
4 Alkhunaizi, E;   5 D'Onofrio, G;   6 Tortora, D;
7 Calì, E;   8 Scudieri, P;   9 Balagura, G;
10 Musante, I;   11 Diana, MC;   12 Pedemonte, M;
13 Vari, MS;   14 Iacomino, M;   15 Riva, A;
16 Chimenz, R;   17 Mangano, GD;   18 Mohammadi, MH;
19 Toosi, MB;   20 Ashrafzadeh, F;   21 Imannezhad, S;
22 Karimiani, EG;   23 Accogli, A;   24 Schiaffino, MC;
25 Maghnie, M;   26 Soler, MA;   27 Echiverri, K;
28 Abrams, CK;   29 Striano, P;   30 Fortuna, S;
31 Maroofian, R;   32 Houlden, H;   33 Zara, F;
34 Fiorillo, C;   35 Salpietro, V;