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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 | Received 12 May 2013, Accepted 13 Aug 2013, Published online: 14 Aug 2013

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