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.

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
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