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A Novel Missense Mutation in TNNI3K Causes Recessively Inhe..:
Ramzan, Shafaq
;
Tennstedt, Stephanie
;
Tariq, Muhammad
...
Genes. 12 (2021) 8 - p. 1282 , 2021
Link:
https://doi.org/10.3390/genes12081282
RT Journal T1
A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family
UL https://suche.suub.uni-bremen.de/peid=cr-10.3390_genes12081282&Exemplar=1&LAN=DE A1 Ramzan, Shafaq A1 Tennstedt, Stephanie A1 Tariq, Muhammad A1 Khan, Sheraz A1 Noor Ul Ayan, Hafiza A1 Ali, Aamir A1 Munz, Matthias A1 Thiele, Holger A1 Korejo, Asad Aslam A1 Mughal, Abdul Razzaq A1 Jamal, Syed Zahid A1 Nürnberg, Peter A1 Baig, Shahid Mahmood A1 Erdmann, Jeanette A1 Ahmad, Ilyas PB MDPI AG YR 2021 SN 2073-4425 JF Genes VO 12 IS 8 SP 1282 LK http://dx.doi.org/https://doi.org/10.3390/genes12081282 DO https://doi.org/10.3390/genes12081282 SF ELIB - SuUB Bremen
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