Sox6 is a candidate gene for p(100H) myopathy, heart block, and sudden neonatal death

The mouse p locus encodes a gene that functions in normal pigmentation. We have characterized a radiation-induced mutant allele of the mouse p locus that is associated with a failure-to-thrive syndrome, in addition to diminished pigmentation. Mice homozygous for this mutant allele, p(100H), show del...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Hagiwara, Nobuko, Klewer, Scott E., Samson, Ricardo A., Erickson, Drew T., Lyon, Mary F., Brilliant, Murray H.
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 2000
Assuntos:	Biological Sciences
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC18189/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10760285/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.97.8.4180
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