Patient Reported Outcomes for Phosphomannomutase 2 Congenital Disorder of Glycosylation (Pmm2-Cdg): Listening to What Matters for the Patients and Health Professionals

AuthID
P-00X-F0C
14
Author(s)
Pascoal, C
·
Ferreira, I
·
Teixeira, C
·
Almeida, E
·
Brasil, S
·
Francisco, R
·
Ligezka, AN
·
Plotkin, H
·
Videira, PA
·
Barros, L
·
Ferreira, VD
Document Type
Article
Year published
2022
Published
in ORPHANET JOURNAL OF RARE DISEASES, ISSN: 1750-1172
Volume: 17, Issue: 1
Indexing
Publication Identifiers
Pubmed: 36309700
Scopus: 2-s2.0-85140976314
Wos: WOS:000876269200001
Source Identifiers
ISSN: 1750-1172
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