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AN ORPHAN PHENOTYPE OF CARDIOGENITAL LAMINOPATHY — MALOUF SYNDROME
Author(s) -
Т. Г. Вайханская,
Л. Н. Сивицкая,
Н. Г. Даниленко,
Т. В. Курушко,
О. Г. Нижникова,
О. Г. Давыденко
Publication year - 2016
Publication title -
rossijskij kardiologičeskij žurnal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.141
H-Index - 14
eISSN - 2618-7620
pISSN - 1560-4071
DOI - 10.15829/1560-4071-2016-11-90-94
Subject(s) - lmna , medicine , progeria , cardiomyopathy , short stature , dysplasia , pathology , genetics , lamin , pediatrics , heart failure , biology , gene , nucleus , psychiatry

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