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Mutational analyses of the signals involved in the subcellular location of DSCR1

BACKGROUND: Down syndrome is the most frequent genetic disorder in humans. Rare cases involving partial trisomy of chromosome 21 allowed a small chromosomal region common to all carriers, called Down Syndrome Critical Region (DSCR), to be determined. The DSCR1 gene was identified in this region and...

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Detalles Bibliográficos
Autores principales: Pfister, Sandra Cristina, Machado-Santelli, Gláucia Maria, Won Han, Sang, Henrique-Silva, Flávio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC128833/
https://www.ncbi.nlm.nih.gov/pubmed/12225619
http://dx.doi.org/10.1186/1471-2121-3-24