Publication | Open Access
Congenital myopathy caused by a novel missense mutation in the CFL2 gene
59
Citations
18
References
2012
Year
Congenital MyopathyMendelian DisorderGenetic DisorderMedicineGeneticsPathologyMolecular GeneticsDisease Gene IdentificationMonogenic DisordersCfl2 GeneNovel Missense MutationClinical Genetics
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