Abstract
A founder transgenic mouse harbored two different integration patterns of a transgene at the same locus, each of which gave rise to a similar autosomal recessive mutation. Mice of the mutant phenotype were of small stature but had normal levels of growth hormone. The disrupted locus was cloned, and a genetic and molecular analysis showed that the insertional mutants were allelic to a spontaneous mutant, pygmy. The mice should be a useful model for the growth hormone-resistant human dwarf syndromes and could lead to a greater understanding of the pathways involved in growth and development.
| Original language | English |
|---|---|
| Pages (from-to) | 967-969 |
| Number of pages | 3 |
| Journal | Science |
| Volume | 247 |
| Issue number | 4945 |
| State | Published - 23 Feb 1990 |