Publication | Open Access
Dominant Mutation of CCDC78 in a Unique Congenital Myopathy with Prominent Internal Nuclei and Atypical Cores
98
Citations
14
References
2012
Year
Mendelian DisorderGenetic DisorderGeneticsUnique Congenital MyopathyMolecular BiologyPathologyProminent Internal NucleiDominant MutationMedicine
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