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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, Louise C. WilsonVolume:
72
Year:
2003
Language:
english
DOI:
10.1086/374566
File:
PDF, 1.06 MB
english, 2003