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Search Results - Oliveira, Mayala Thayrine de J S
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Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis
by
da Silva-Batista, Jemima A
,
Marques, Jr, Wilson
,
Oliveira, Mayala Thayrine de J S
,
Lins, Lucas Vergne C
,
Galvão, Adilson Junior P
,
Miguel, Diego Santana Chaves G
,
Machado-Costa, Marcela Câmara
Published in
Journal of human genetics
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Journal Of Human Genetics
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Amyloidosis
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Amyloidosis, Familial - Genetics
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Amyloidosis, Familial - Physiopathology
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Brazil
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Cardiomyopathies - Genetics
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Cardiomyopathies - Physiopathology
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Cardiomyopathy
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Disease
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Disease Progression
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Edema
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Erectile Dysfunction
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Family Medical History
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Genetics & Heredity
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Heterozygote
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Humans
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Life Sciences & Biomedicine
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Male
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Middle Aged
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Mutation
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Patients
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Springer Nature
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Ezb Electronic Journals Library
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Springer Link Contemporary (1997 - Present)
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