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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...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1867825/ https://ncbi.nlm.nih.gov/pubmed/17439653 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-8-16 |
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