Reference Expression Profile of Three
Marfan syndrome
alternative splicing
clinical variability
fibrilline-1
isoforms
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
11 02 2019
11 02 2019
Historique:
received:
07
01
2019
revised:
30
01
2019
accepted:
06
02
2019
entrez:
14
2
2019
pubmed:
14
2
2019
medline:
14
2
2019
Statut:
epublish
Résumé
Marfan syndrome (MFS) is a rare connective tissue disorder mainly due to mutations in the
Identifiants
pubmed: 30754709
pii: genes10020128
doi: 10.3390/genes10020128
pmc: PMC6409622
pii:
doi:
Substances chimiques
FBN1 protein, human
0
Fibrillin-1
0
Protein Isoforms
0
RNA, Messenger
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Déclaration de conflit d'intérêts
The authors declare no conflicts of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.
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