Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse. [electronic resource]
Producer: 19981028Description: 157-62 p. digitalISSN:- 1061-4036
- Amino Acid Sequence
- Animals
- Chromosome Mapping
- Chromosomes, Human, Pair 10
- Codon, Terminator
- Consanguinity
- Genetic Linkage
- Humans
- Mice
- Molecular Sequence Data
- Mutation
- Osteochondrodysplasias -- genetics
- Pedigree
- Phosphotransferases (Alcohol Group Acceptor) -- genetics
- Protein Processing, Post-Translational
- Sequence Alignment
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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