People also looked at
Top bar navigation
Assessing the Functional Significance of Novel and Rare Variants of the SLC26A4 Gene Found in Patients with Hearing Loss by Minigene Assay
A novel splicing variant in NBAS identified by minigene assay causes infantile liver failure syndrome type 2
Novel pathogenic splicing mutation in COL11A1 in a patient with Stickler syndrome verified by minigene splicing assay