Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome.

Saved in:
Bibliographic Details
Title: Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome.
Authors: Govindaraj, Geeta Madathil1,2 (AUTHOR) vinods@igib.in, Jain, Abhinav3,4 (AUTHOR), Peethambaran, Geetha1 (AUTHOR), Bhoyar, Rahul C.3 (AUTHOR), Vellarikkal, Shamsudheen Karuthedath3 (AUTHOR), Ganapati, Arvind5 (AUTHOR), Sandhya, Pulukool5 (AUTHOR), Edavazhippurath, Athulya1,6 (AUTHOR), Dhanasooraj, Dhananjayan6 (AUTHOR), Puthenpurayil, Jayakrishnan Machinary1 (AUTHOR), Chakkiyar, Krishnan1 (AUTHOR), Mishra, Anushree3 (AUTHOR), Batra, Arushi3,4 (AUTHOR), Punnen, Anu7 (AUTHOR), Kumar, Sathish7 (AUTHOR), Sivasubbu, Sridhar3,4 (AUTHOR), Scaria, Vinod3,4 (AUTHOR) vinods@igib.in
Source: PLoS ONE. 8/21/2020, Vol. 15 Issue 8, p1-16. 16p.
Database: Academic Search Ultimate
Full text is not displayed to guests.
Description
ISSN:19326203
DOI:10.1371/journal.pone.0237999