Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy.
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Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy.
description
2016 nî lūn-bûn
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2016年の論文
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2016年論文
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2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
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2016年论文
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name
Discovery of a potentially del ...... nd restrictive cardiomyopathy.
@en
type
label
Discovery of a potentially del ...... nd restrictive cardiomyopathy.
@en
prefLabel
Discovery of a potentially del ...... nd restrictive cardiomyopathy.
@en
P2093
P2860
P356
P1476
Discovery of a potentially del ...... and restrictive cardiomyopathy
@en
P2093
Blake J Salvador
Elizabeth A Geiger
Ellen R Elias
Jean L Cavanaugh
Kathryn C Chatfield
Shelley D Miyamoto
Tamim H Shaikh
P2860
P304
P356
10.1101/MCS.A000844
P577
2016-05-01T00:00:00Z