Whole-exome sequencing reveals a novel homozygous mutation in the COQ8B gene associated with nephrotic syndrome
Crossref DOI link: https://doi.org/10.1038/s41598-021-92023-3
Published Online: 2021-06-25
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Fareed, Mohd
Makkar, Vikas
Angral, Ravi
Afzal, Mohammad
Singh, Gurdarshan
Text and Data Mining valid from 2021-06-25
Version of Record valid from 2021-06-25
Article History
Received: 2 February 2021
Accepted: 18 May 2021
First Online: 25 June 2021
Competing interests
: The authors declare no competing interests.