[Ehlers-Danlos syndrome type I: importance of genetic diagnosis]
An Pediatr (Barc)
.
2010 Feb;72(2):157-9.
doi: 10.1016/j.anpedi.2009.11.013.
Epub 2010 Jan 29.
[Article in Spanish]
Authors
C Lobete Prieto
1
,
I Llano Rivas
,
J Fernández Toral
,
P Madero Barrajón
Affiliation
1
Unidad de Genética, Hospital Universitario Central de Asturias, Oviedo, España. carloslobete@hotmail.com <carloslobete@hotmail.com>
PMID:
20116353
DOI:
10.1016/j.anpedi.2009.11.013
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Ehlers-Danlos Syndrome / genetics*
Female
Humans
Point Mutation / genetics
Young Adult