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Mamta N. Muranjan
Mamta N. Muranjan
King Edward Memorial Hospital
Medicine
Internal medicine
Pediatrics
Missense mutation
Disease
4
Papers
11
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0
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Late Onset Pompe Disease in India – beyond the Caucasian phenotype
2021
Neuromuscular Disorders
Ratna Dua-Puri
Nitika Setia
N. Vinu
Sujatha Jagadeesh
Sheela Nampoothiri
Neerja Gupta
Mamta N. Muranjan
Meenakshi Bhat
Katta M. Girisha
Madhulika Kabra
Jyotsna Verma
Divya C. Thomas
Ishpreet K. Biji
Jayarekha Raja
Ravinder Makkar
Ishwar C. Verma
Priya S. Kishnani
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Diagnosis is in the Eye of the Beholder: Barriers to Early Diagnosis of Mucopolysaccharidosis in Children in India
2020
Journal of pediatric genetics
Meenu Grewal
Mamta N. Muranjan
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Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1
2020
Journal of pediatric genetics
Parag M. Tamhankar
Lakshmi Vasudevan
Pratima Kondurkar
Sarfaraj Niazi
Rita Christopher
Dhaval I Solanki
Pooja J. Dholakia
Mamta N. Muranjan
Mahesh Kamate
Umesh Kalane
Jayesh Sheth
Vasundhara Parag Tamhankar
Reena Gulati
Madhavi Vasikarla
Sumita Danda
Shaik Mohammad Naushad
Katta M. Girisha
Shekhar Patil
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Clinical and Molecular Disease Spectrum and Outcomes in Patients with Infantile-Onset Pompe Disease
2019
The Journal of Pediatrics
Neerja Gupta
Zoheb B. Kazi
Sheela Nampoothiri
Sujatha Jagdeesh
Madhulika Kabra
Ratna Dua-Puri
Mamta N. Muranjan
Mani Kalaivani
Catherine Rehder
Deeksha Bali
Ishwar C. Verma
Priya S. Kishnani
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Citations (10)
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