ArticleAmerican journal of human genetics2003

Analysis of GNAS1 and overlapping transcripts identifies the parental origin of mutations in patients with sporadic Albright hereditary osteodystrophy and reveals a model system in which to observe the effects of splicing mutations on translated and untranslated messenger RNA.

Sarah J Rickard et al.PubMed ↗Full text ↗Publisher ↗

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