Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms.
about
ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features.ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and establish that ALPK3 deficiency underlies familial cardiomyopathy.
P2860
Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
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2016年學術文章
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2016年學術文章
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name
Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms.
@en
Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms.
@nl
type
label
Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms.
@en
Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms.
@nl
prefLabel
Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms.
@en
Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms.
@nl
P2093
P2860
P1476
Pediatric Cardiomyopathy: New Insight Into Potential Disease Mechanisms.
@en
P2093
Luisa Mestroni
Mary E Sweet
Matthew R G Taylor
P2860
P304
P356
10.1016/J.JACC.2015.11.030
P407
P577
2016-02-01T00:00:00Z