Article
Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets.
Genome research - 1 Jun 1997
Francis F, Strom T M, Hennig S, Böddrich A, Lorenz B, Brandau O, Mohnike K L, Cagnoli M, Steffens C, Klages S, Borzym K, Pohl T, Oudet C, Econs M J, Rowe P S, Reinhardt R, Meitinger T, Lehrach H
Abstract excerpt
No abstract is available from the source.
Topics
- Cloning, Molecular
- Codon, Nonsense
- Exons
- Female
- Frameshift Mutation
- Genetic Variation
- Humans
- Hypophosphatemia, Familial
- Introns
- Male
- Molecular Sequence Data
- Mutation
- Neprilysin
- PHEX Phosphate Regulating Neutral Endopeptidase
- Pedigree
- Proteins
- Sequence Analysis, DNA
- Sequence Deletion