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Q36859420-79415F6F-5496-4377-B50A-808AF1F1B9BF
Q36859420-79415F6F-5496-4377-B50A-808AF1F1B9BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36859420-79415F6F-5496-4377-B50A-808AF1F1B9BF
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.
P2860
Q36859420-79415F6F-5496-4377-B50A-808AF1F1B9BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36859420-79415F6F-5496-4377-B50A-808AF1F1B9BF
rank
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type
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wasDerivedFrom
a6af9474864390acbfefc3c59b99b1c1ed245dbf
P2860
Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline.