Publication | Open Access
A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI
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Citations
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References
2008
Year
Rare DiseasesMendelian DisorderGenetic DisorderMedicineGeneticsDegenerative DiseaseMedical GeneticsNeurologyNeuroscienceDisease Gene IdentificationNovel Pomt2 MutationNeuropathologyNeuromuscular PathologyNormal Brain MriNeurogenetics
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