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383205
383205
http://dx.doi.org/10.1086/383205
Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly
P356
Q24533381-97678748-8CE1-4C4B-AD54-418AA8C10CDC
P356
383205
http://dx.doi.org/10.1086/383205