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Novel RNASEH2C mutation in multiple members of a large family: insights into phenotypic spectrum of Aicardi-Goutières Syndrome
Lhamtsho, Dema, Rajesh, Uddandam, Saxena, Apoorv, Bhardwaj, Girish, Sondhi, VishalVolume:
2
Journal:
BMJ Neurology Open
DOI:
10.1136/bmjno-2019-000018
Date:
January, 2020
File:
PDF, 923 KB
2020