Manojkumar Kumaran
1PUBLICATIONS
6CO-AUTHORS

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Publications (1)
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|Nov 09, 2021
Clinical reassessments and whole-exome sequencing uncover novel <i>BEST1</i> mutation associated with bestrophinopathy phenotype.Susmita Chowdhury, Roopam Duvesh, Manojkumar Kumaran
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