Novel FHL1 mutation variant identified in a patient with...

BMC Medical Genetics 2020 / 12 Vol. 21; Iss. 1

Novel FHL1 mutation variant identified in a patient with nonobstructive hypertrophic cardiomyopathy and myopathy – a case report

Giucă, Adrian, Mitu, Cristina, Popescu, Bogdan Ovidiu, Bastian, Alexandra Eugenia, Capşa, Răzvan, Mursă, Adriana, Rădoi, Viorica, Popescu, Bogdan Alexandru, Jurcuţ, Ruxandra
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Volume:
21
Journal:
BMC Medical Genetics
DOI:
10.1186/s12881-020-01131-w
Date:
December, 2020
File:
PDF, 1.19 MB
2020
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