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The identification of PAX7 variants and a potential role of muscle development dysfunction in congenital scoliosis.
Cell Regen. 2022 May 2;11(1):16. doi: 10.1186/s13619-022-00116-9.
Cell Regen. 2022.
PMID: 35499749
Free PMC article.
No abstract available.
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome.
Li Z, Zhao S, Cai S, Zhang Y, Wang L, Niu Y, Li X, Hu J, Chen J, Wang S, Wang H, Liu G, Tian Y, Wu Z, Zhang TJ; DISCO (Deciphering Disorders Involving Scoliosis and COmorbidities) study; Wang Y, Wu N.
Li Z, et al.
BMC Musculoskelet Disord. 2020 Apr 11;21(1):220. doi: 10.1186/s12891-020-03229-x.
BMC Musculoskelet Disord. 2020.
PMID: 32278351
Free PMC article.
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