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Radharamadevi Akella

3PUBLICATIONS
4CO-AUTHORS
Gene mappingNeurology and neuromuscular diseasesInfant and child health
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Publications (3)

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|May 09, 2024
SWI/SNF-Related <i>SMARCA2</i> Gene Mutation Associated with Nicolaides-Baraitser's Syndrome: Follow-up Study.

Radharamadevi Akella

|Jul 17, 2021
Functional characterization of novel variants in SMPD1 in Indian patients with acid sphingomyelinase deficiency.

Dipti Deshpande, Shailesh Kumar Gupta, Asodu Sandeep Sarma

|Feb 15, 2021
A rare case of fatty acyl-CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype.

Akella Radha Rama Devi, Shaik Mohammad Naushad, Romit Jain

Pageof 1

Frequent Collaborators

1 joint publications

Prajnya Ranganath

1 joint publications

Shagun Aggarwal

1 joint publications

Mamta Muranjan

1 joint publications

Ashwin B Dalal

Frequent Collaborators

1 joint publications

Prajnya Ranganath

1 joint publications

Shagun Aggarwal

1 joint publications

Mamta Muranjan

1 joint publications

Ashwin B Dalal

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