M. Muranjan
发表
P. Vijayalakshmi,
M. Muranjan,
2014,
The Indian Journal of Pediatrics.
M. Kabra,
S. Phadke,
K. Mandal,
2021,
Human mutation.
S. Nampoothiri,
A. Bavdekar,
Varun Khanna,
2014,
Journal of Human Genetics.
S. Kapoor,
S. Phadke,
K. Girisha,
2019,
BMC Medical Genetics.
B. Vundinti,
M. Muranjan,
T. Chaudhari,
2010,
Indian pediatrics.
Smita G. Patil,
M. Muranjan,
2016,
Indian Pediatrics.
M. Muranjan,
2016
.
M. Bashyam,
K. Lahiri,
M. Muranjan,
2012,
Indian pediatrics.
S. Karande,
M. Muranjan,
S. Mhatre,
2021,
BMJ Case Reports.
M. Kabra,
K. Girisha,
S. Nampoothiri,
2021,
Neuromuscular Disorders.
S. Phadke,
K. Girisha,
A. Shukla,
2021,
American journal of medical genetics. Part A.
S. Bavdekar,
Himanshu Batra,
Suresh Birajdar,
2005,
International journal of pediatric otorhinolaryngology.
G. Mortier,
K. Girisha,
A. Shukla,
2018,
Human mutation.
F. Sheth,
J. Sheth,
K. Shah,
2017,
BMC Medical Genetics.
S. Karande,
R. Parikh,
M. Muranjan,
2014,
Pediatric neurology.
p.Arg69Trp in RNASEH2C is a founder variant in three Indian families with Aicardi–Goutières syndrome
K. Girisha,
A. Shukla,
M. Hebbar,
2018,
American journal of medical genetics. Part A.
S. Karande,
M. Muranjan,
S. Mahalawat,
2021,
Journal of postgraduate medicine.
N. Dipak,
M. Muranjan,
Shilpa Pandya,
2022,
NeoReviews.
S. Bavdekar,
M. Ursekar,
M. Muranjan,
2001,
Indian Pediatrics.
S. Nampoothiri,
A. Bavdekar,
Varun Khanna,
2014,
Journal of Human Genetics.
K. Girisha,
S. Patil,
M. Muranjan,
2023,
American journal of medical genetics. Part A.
N. Gogtay,
M. Muranjan,
S. Mhatre,
2023,
Indian journal of pediatrics.
S. Kapoor,
S. Phadke,
K. Girisha,
2019,
BMC Medical Genetics.
M. Muranjan,
A. Taksande,
Priyanka Hampe,
2024,
Cureus.
S. Nampoothiri,
F. Sheth,
J. Sheth,
2024,
Orphanet journal of rare diseases.