Archive
Year
Volume(Issue)
Issues
Journal Article
Download
فارسی Version
A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: Clinical course and response to riboflavin
BMC MEDICAL GENETICS
Year:
Volume:
Issue:
Pages:
Citations:
Views:
Downloads:
more
View 53
Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes
View 48
A novel homozygous frameshift mutation in the SLC29A3 gene: a new case report and review of literature
View 11