Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome.
Saved in:
| 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.
Login for full access.
|
|
Be the first to leave a comment!