Publication | Closed Access
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)
260
Citations
14
References
2003
Year
Extraocular MusclesCongenital FibrosisFibrosisMendelian DisorderSkeletal MuscleGenetic DisorderMedicineGeneticsPathologyKinesin Kif21aNeuromuscular PathologyConnective Tissue Disease
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