Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC gene.

The 5q- syndrome is a myelodysplastic syndrome with the 5q deletion as the sole karyotypic abnormality. The human ATX1 homologue (HAH1), encodes a copper-binding protein with a role in antioxidant defence. We have mapped this gene to the 3 Mb critical region of gene loss of the 5q- syndrome within 5...

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Библиографические подробности
Главные авторы: Boultwood, J, Strickson, A, Jabs, E, Cheng, J, Fidler, C, Wainscoat, J
Формат: Journal article
Язык:English
Опубликовано: 2000