Recombination of 4p16 DNA markers in an unusual family with Huntington disease

The Huntington disease (HD) mutation has been localized to human chromosome 4p16, in a 6-Mb region between the D4S10 locus and the 4p telomere. In a report by Robbins et al., a family was identified in which an affected individual failed to inherit three alleles within the 6-Mb region originating fr...

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Autores principales: Pritchard, Catrin, Zhu, Ning, Zuo, Jian, Bull, Laura, Pericak-Vance, Margaret A., Vance, Jeffery M., Roses, Allen D., Milatovich, Athena, Francke, Uta, Cox, David R., Myers, Richard M.
Formato: Artigo
Lenguaje:Inglês
Publicado: 1992
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Original Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682573/
https://ncbi.nlm.nih.gov/pubmed/1350884
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