Identification of two novel deletion mutations within the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophy. [electronic resource]
Producer: 19991006Description: 3254-9 p. digitalISSN:- 0021-972X
- Amino Acid Sequence
- Base Sequence
- Female
- Fibrous Dysplasia, Polyostotic -- genetics
- Frameshift Mutation
- GTP-Binding Protein alpha Subunits, Gs -- chemistry
- Gene Deletion
- Heterozygote
- Humans
- Infant, Newborn
- Male
- Pedigree
- Polymerase Chain Reaction
- Pseudohypoparathyroidism -- genetics
- Pseudopseudohypoparathyroidism -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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