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pro vyhledávání: '"Mers Siqueira"'
Autor:
A.C. Campos-de-Carvalho, Ips Bezerra, Mers Siqueira, Raq Barbosa, Tais Hanae Kasai-Brunswick, Eduardo Back Sternick
Publikováno v:
Cytotherapy. 23:9-10
Background PRKAG2 cardiomyopathy is an autosomal dominant syndrome due to mutation in PRKAG2 gene, which encodes the γ2 subunit of the adenosine monophosphate (AMP)-activated protein kinase (AMPK). PRKAG2 syndrome leads to intracellular cardiomyocyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdb7723bcf09dd291273c4338eaf439a
https://doi.org/10.1016/j.jcyt.2021.02.033
https://doi.org/10.1016/j.jcyt.2021.02.033
