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Whole-exome sequencing identified compound heterozygous var..:
Mahdavi, Mohammad
;
Mohsen-Pour, Neda
;
Maleki, Majid
...
Cardiology in the Young. 32 (2021) 9 - p. 1462-1467 , 2021
Link:
https://doi.org/10.1017/s1047951121004455
RT Journal T1
Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family
UL https://suche.suub.uni-bremen.de/peid=cr-10.1017_s1047951121004455&Exemplar=1&LAN=DE A1 Mahdavi, Mohammad A1 Mohsen-Pour, Neda A1 Maleki, Majid A1 Hesami, Mahshid A1 Naderi, Niloofar A1 Houshmand, Golnaz A1 Rasouli Jazi, Hamid R. A1 Shahzadi, Hossein A1 Kalayinia, Samira PB Cambridge University Press (CUP) YR 2021 SN 1047-9511 SN 1467-1107 JF Cardiology in the Young VO 32 IS 9 SP 1462 OP 1467 LK http://dx.doi.org/https://doi.org/10.1017/s1047951121004455 DO https://doi.org/10.1017/s1047951121004455 SF ELIB - SuUB Bremen
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