Publication | Closed Access
Oculopharyngeal muscular dystrophy in a Japanese family with a short GCG expansion (GCG)11 in PABP2 gene
32
Citations
8
References
2000
Year
Rare DiseasesDevelopmental BiologyPabp2 GeneMendelian DisorderGenetic DisorderJapanese FamilyGeneticsMedicineDegenerative DiseaseMolecular GeneticsDisease Gene IdentificationShort Gcg ExpansionNeuromuscular Pathology
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