Publication | Closed Access
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
522
Citations
21
References
2001
Year
Mendelian DisorderGenetic DisorderGeneticsMolecular BiologyDegenerative DiseaseMolecular GeneticsDisease Gene IdentificationMedicine
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