Viable phenotype of ILNEB syndrome without nephrotic impairment in siblings heterozygous for unreported integrin alpha3 mutations
Elisa Adele Colombo,Luigina Spaccini,Ludovica Volpi…Volume:
11
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-016-0514-z
Date:
December, 2016
File:
PDF, 1.39 MB
english, 2016