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Mehta, S. et al. (n.d.). Genotype–phenotype studies of VCP‐associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia. Clinical genetics. pp. 422-431. [Online].
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Mehta, S. et al. (n.d.). Genotype–phenotype studies of VCP‐associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia. Clinical genetics. pp. 422-431. [Online].