Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3

Literals

fabio:hasPublicationYear
- 2015
ou:vecesCitado
- 19
ou:eid
- 2-s2.0-84979733210
ou:bibtex
- @article{PMID:26029709, title = {Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3.}, author = {Joshi R and Shvartsman M and Morán E and Lois S and Aranda J and Barqué A and de la Cruz X and Bruguera M and Vagace JM and Gervasini G and Sanz C and Sánchez M}, doi = {10.1002/mgg3.136}, journal = {Molecular genetics & genomic medicine}, month = {05}, year = {2015} }
ou:tipoPublicacion
- Note
dcterms:creator
- Joshi R.
vcard:url
- https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979733210&origin=inward
bibo:eissn
- 2324-9269
ou:urlOrcid
- http://europepmc.org/abstract/med/26029709
dcterms:publisher
- Molecular Genetics and Genomic Medicine
dcterms:title
- Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3
dcterms:contributor
- Joshi R. et al.
bibo:page_range
- 221-232
vivo:identifier
- 2015-242
ou:urlScopus
- https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979733210&origin=inward
bibo:doi
- 10.1002/mgg3.136
bibo:volume
- 3