Gene Location for Molybdenum Cofactor Deficiency
DOI:
https://doi.org/10.15844/pedneurbriefs-12-8-3Keywords:
Molybdenum Cofactor Deficiency, Opisthotonus, Xanthine DehydrogenaseAbstract
Linkage of a molybdenum cofactor deficiency (MoCoD) gene to an 8-cM region on chromosome 6p21.3 has been localized by homozygosity mapping in 2 consanguineous affected kindreds of Israeli-Arab origin, including 5 patients, at the Department of Genetics, Tamkin Research Facility, Technion-Israel Institute of Technology, Haifa, Israel.Published
1998-08-01
Issue
Section
Metabolic Disorders
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Copyright (c) 1998 The Author(s)
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