Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome. [electronic resource]
Producer: 19970710Description: 1384-8 p. digitalISSN:- 0002-9297
- Amino Acid Sequence
- Cells, Cultured
- Conserved Sequence
- Exons
- Fibroblasts
- Frameshift Mutation
- Golgi Apparatus -- enzymology
- Humans
- Lymphocytes
- Male
- Molecular Sequence Data
- Mutation
- Oculocerebrorenal Syndrome -- genetics
- Phosphoric Monoester Hydrolases -- chemistry
- Point Mutation
- Polymerase Chain Reaction
- Polymorphism, Single-Stranded Conformational
- Protein Biosynthesis
- Proteins -- chemistry
- Sequence Alignment
- Sequence Deletion
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.