PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy –Consequences in Clinical Diagnosis and Genetic Counselling
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E. Malfatti | N. Romero | B. Eymard | M. Fardeau | C. Trollet | T. Gidaro | P. Richard | G. Brochier | L. Demay | J. Saint-Guily | F. Tom | Pascal Lafor | Marie-Laure Martin-N | Guilhem Sol | X. Ferrer-Monasterio | J. L. Saint-Guily | Fernando Tom