Whole exome sequencing identifies a novel intron heterozygous mutation in TSC2 responsible for tuberous sclerosis complex
Crossref DOI link: https://doi.org/10.1038/s41598-019-38898-9
Published Online: 2019-03-14
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Ye, Yicong
Zeng, Yong
Text and Data Mining valid from 2019-03-14
Version of Record valid from 2019-03-14
Article History
Received: 6 July 2018
Accepted: 21 December 2018
First Online: 14 March 2019
Competing Interests
: The authors declare no competing interests.