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

Crossref DOI link: https://doi.org/10.1186/s40662-021-00243-5

Published Online: 2021-05-06

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Viswarubhiny, Sriee

Anjanamurthy, Rupa

Vanniarajan, Ayyasamy

Bharanidharan, Devarajan

Perumalsamy, Vijayalakshmi

Sundaresan, Periasamy
Funding

Funding for this research was provided by:

Department of Biotechnology, India (BT/NNT/28/SP18830/2018)
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Article History

Received: 16 October 2020

Accepted: 14 April 2021

First Online: 6 May 2021

Declarations

:

: This study was approved by the Institutional Ethics Committee of Aravind Eye Hospital, Madurai, Tamil Nadu, India (IRB2016017BAS).

: Not applicable.

: None of the authors have any proprietary interests or conflicts of interest related to this submission.

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