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A single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab mice
BACKGROUND: The long bone abnormality (lbab) mouse is a new autosomal recessive mutant characterized by overall smaller body size with proportionate dwarfing of all organs and shorter long bones. Previous linkage analysis has located the lbab mutation on chromosome 1 between the markers D1Mit9 and D...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867825/ https://www.ncbi.nlm.nih.gov/pubmed/17439653 http://dx.doi.org/10.1186/1471-2156-8-16 |