Radharamadevi Akella

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

|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

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