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Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosis
by
Johansson, Josefin
,
Frykholm, Carina
,
Ericson, Katharina
,
Kazamia, Kalliopi
,
Lindberg, Amanda
,
Mulaiese, Nancy
,
Falck, Geir
,
Gustafsson, Per‐Erik
,
Lidéus, Sarah
,
Gudmundsson, Sanna
,
Ameur, Adam
,
Bondeson, Marie‐Louise
,
Wilbe, Maria
Published in
American journal of medical genetics. Part A
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American Journal Of Medical Genetics. Part A
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Actin
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Autopsy
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Cardiomegaly - Genetics
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Cardiomegaly - Metabolism
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Cardiomegaly - Pathology
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Cardiomyopathy
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Dilated Cardiomyopathy
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Disc Protein
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Endocardial Fibroelastosis
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Endocardial Fibroelastosis - Genetics
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Endocardial Fibroelastosis - Metabolism
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Endocardial Fibroelastosis - Pathology
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Female
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Fetuses
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Genetics & Heredity
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Heart
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Heterozygotes
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Humans
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Immunohistochemistry
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Lethal
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Wiley-Blackwell Journals
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