Gene Location for Molybdenum Cofactor Deficiency
Abstract
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.
DOI: https://doi.org/10.15844/pedneurbriefs-12-8-3 | Journal eISSN: 2166-6482
Language: English
Page range: 58 - 59
Published on: Aug 1, 1998
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 1998 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.