MYL2 -associated congenital fiber-type...

Molecular Case Studies 2019 / 05

MYL2 -associated congenital fiber-type disproportion and cardiomyopathy with variants in additional neuromuscular disease genes; the dilemma of panel testing

Marttila, Minttu, Win, Wathone, Al-Ghamdi, Fouad, Abdel-Hamid, Hoda Z., Lacomis, David, Beggs, Alan H.
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Language:
english
Journal:
Molecular Case Studies
DOI:
10.1101/mcs.a004184
Date:
May, 2019
File:
PDF, 1.16 MB
english, 2019
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