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FANCD2 Western blot as a diagnostic tool for Brazilian patients with Fanconi anemia
Fanconi anemia is a rare hereditary disease showing genetic heterogeneity due to a variety of mutations in genes involved in DNA repair pathways, which may lead to different clinical manifestations. Phenotypic variability makes diagnosis difficult based only on clinical manifestations, therefore lab...
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Hlavní autoři: | , , , , , , , , |
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Médium: | Artigo |
Jazyk: | Inglês |
Vydáno: |
Associação Brasileira de Divulgação Científica
2009-03-01
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Edice: | Brazilian Journal of Medical and Biological Research |
Témata: | |
On-line přístup: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2009000300004 |
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