Additional file 1 of Clinical exome sequencing facilitates the understanding of genetic heterogeneity in Leber congenital amaurosis patients with variable phenotype in southern India

Additional file 1 of Clinical exome sequencing facilitates the understanding of genetic heterogeneity in Leber congenital amaurosis patients with variable phenotype in southern India

Additional file 1: Supplementary Table S1. Primer sequences used for the mutation validation by Sanger sequencing.

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Sriee Viswarubhiny, Anjanamurthy, Rupa, Ayyasamy Vanniarajan, Devarajan Bharanidharan, Vijayalakshmi Perumalsamy, Periasamy Sundaresan
Format: Dataset
Sprache:eng
Schlagworte:
FOS: Biological sciences
Genetics
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Additional file 1: Supplementary Table S1. Primer sequences used for the mutation validation by Sanger sequencing.
DOI:10.6084/m9.figshare.14552105