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Sony Mohan
Sony Mohan
Christian Medical College & Hospital
Medicine
Mutation
Exon
Gene
Subfamily
3
Papers
1
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0
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Long-Term Follow-Up of a Patient with a De Novo p.Arg769Cys Mutation in the ATP1A3 Gene
2021
Movement Disorders Clinical Practice
Anjali Chouksey
Asish Vijayaraghavan
Sony Mohan
Srija Inturi
A. T. Prabhakar
Vivek Mathew
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Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India.
2020
Clinical Rheumatology
Sumita Danda
Sony Mohan
Prabavathi Devaraj
Atanu Kumar Dutta
Sheela Nampoothiri
Dhanya Yesodharan
Shubha R. Phadke
Anil Jalan
K. Thangaraj
Ishwar C. Verma
Debashish Danda
Isaac Jebaraj
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Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India
2019
The National Medical Journal of India
Sony Mohan
Sumita Danda
Sarah Mathai
Anna Simon
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