Positional dissociation between the genetic mutation responsible for pseudohypoparathyroidism type Ib and the associated methylation defect at exon A/B: evidence for a long-range regulatory element within the imprinted GNAS1 locus
Bastepe, M, Pincus, J E, Sugimoto, T, Tojo, K, Kanatani, M, Azuma, Y, Kruse, K, Rosenbloom, A L, Koshiyama, H, Jüppner, H
Published in Human molecular genetics (01.06.2001)
Published in Human molecular genetics (01.06.2001)
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