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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.

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Description scientific article published on May 2016
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author: Hung-Chun Yu  Tamim H Shaikh  Curtis R Coughlin Ii 

Publication date May 1, 2016
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