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Rare Diseases
Volume 1, 2013 - Issue 1
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Research Paper
A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice
Lea Tuzovic New York Presbyterian Hospital; New York, NY USA
, Lan Yu Department of Pediatrics; Columbia University Medical Center; New York, NY USA
, Wenqi Zeng Ambry Genetics; Aliso Viejo, CA USA
, Xiang Li Ambry Genetics; Aliso Viejo, CA USA
, Hong Lu Ambry Genetics; Aliso Viejo, CA USA
, Hsiao-Mei Lu Ambry Genetics; Aliso Viejo, CA USA
, Kelly DF Gonzalez Ambry Genetics; Aliso Viejo, CA USA
& Wendy K Chung Department of Pediatrics; Columbia University Medical Center; New York, NY USACorrespondence[email protected]
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Article: e26144
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Received 12 May 2013, Accepted 13 Aug 2013, Published online: 14 Aug 2013
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