Lipoid proteinosis: rare case confirmed by ECM1 mutation detection
Int J Pediatr Otorhinolaryngol
.
2014 Dec;78(12):2314-5.
doi: 10.1016/j.ijporl.2014.09.025.
Epub 2014 Oct 2.
Authors
Tatiana F Almeida
1
,
Diogo C Soares
2
,
Caio R Quaio
3
,
Rachel S Honjo
4
,
Débora R Bertola
5
,
John A McGrath
6
,
Chong A Kim
7
Affiliations
1
Genetics Unit, Child's Institute, University of São Paulo, São Paulo, Brazil. Electronic address: tatifalmeida@gmail.com.
2
Genetics Unit, Child's Institute, University of São Paulo, São Paulo, Brazil. Electronic address: diogo.soares@hc.fm.usp.br.
3
Genetics Unit, Child's Institute, University of São Paulo, São Paulo, Brazil. Electronic address: caio.quaio@hc.fm.usp.br.
4
Genetics Unit, Child's Institute, University of São Paulo, São Paulo, Brazil. Electronic address: rachel.honjo@gmail.com.
5
Genetics Unit, Child's Institute, University of São Paulo, São Paulo, Brazil. Electronic address: debora.bertola@usp.br.
6
St John's Institute of Dermatology, King's College London, Guy's Campus, London, UK. Electronic address: john.mcgrath@kcl.ac.uk.
7
Genetics Unit, Child's Institute, University of São Paulo, São Paulo, Brazil. Electronic address: chong.kim@hc.fm.usp.br.
PMID:
25441608
DOI:
10.1016/j.ijporl.2014.09.025
No abstract available