Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss

Title
Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss
Authors
Keywords
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Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 90, Issue 2, Pages 201-216
Publisher
Elsevier BV
Online
2012-01-20
DOI
10.1016/j.ajhg.2011.12.004

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