Functional Characterization of a Novel Truncating Mutation in Lamin A/C Gene in a Family with a Severe Cardiomyopathy with Conduction Defects.
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Functional Characterization of a Novel Truncating Mutation in Lamin A/C Gene in a Family with a Severe Cardiomyopathy with Conduction Defects.
description
2017 nî lūn-bûn
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2017年の論文
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name
Functional Characterization of ...... pathy with Conduction Defects.
@en
Functional Characterization of ...... pathy with Conduction Defects.
@nl
type
label
Functional Characterization of ...... pathy with Conduction Defects.
@en
Functional Characterization of ...... pathy with Conduction Defects.
@nl
prefLabel
Functional Characterization of ...... pathy with Conduction Defects.
@en
Functional Characterization of ...... pathy with Conduction Defects.
@nl
P2093
P356
P1476
Functional Characterization of ...... pathy with Conduction Defects.
@en
P2093
Elisabetta Zachara
Federica Re
Giuseppe Procino
Irene Bottillo
Maria Grazia Mola
Maria Svelto
Martina Lipari
Paola Grammatico
Roberta De Zio
Serena Milano
P304
P356
10.1159/000485651
P577
2017-12-04T00:00:00Z