Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia.

Autor: Jain, Abhinav1,2 (AUTHOR), Govindaraj, Geeta Madathil3,4 (AUTHOR) vinods@igib.in, Edavazhippurath, Athulya3,5 (AUTHOR), Faisal, Nabeel3 (AUTHOR), Bhoyar, Rahul C.1 (AUTHOR), Gupta, Vishu1,2 (AUTHOR), Uppuluri, Ramya6 (AUTHOR), Manakkad, Shiny Padinjare3 (AUTHOR), Kashyap, Atul1 (AUTHOR), Kumar, Anoop1 (AUTHOR), Divakar, Mohit Kumar1,2 (AUTHOR), Imran, Mohamed1,2 (AUTHOR), Sawant, Sneha7 (AUTHOR), Dalvi, Aparna7 (AUTHOR), Chakyar, Krishnan3 (AUTHOR), Madkaikar, Manisha7 (AUTHOR), Raj, Revathi6 (AUTHOR), Sivasubbu, Sridhar1,2 (AUTHOR) vinods@igib.in, Scaria, Vinod1,2 (AUTHOR) vinods@igib.in
Zdroj: PLoS ONE. 7/12/2021, Vol. 16 Issue 7, p1-16. 16p.
Databáze: Academic Search Ultimate
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