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[2] "Biallelic mutations in FKBP14 may result in a recessive form of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, hearing loss, and, possibly, an increased risk for vascular complications." [2] [14] An EDS Types Chart [15] with AD/AR inheritance pattern (IP), genetic basis, and protein involved are provided by The Ehlers Danlos Society

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