Gene Location for Molybdenum Cofactor Deficiency
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 Inst...
Saved in:
Main Author: | J Gordon Millichap (Author) |
---|---|
Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
1998-08-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Molybdenum-Cofactor Deficiency and Seizures
by: J Gordon Millichap
Published: (1993) -
Early Neuroimaging in Molybdenum Cofactor Deficiency
by: J Gordon Millichap, et al.
Published: (2014) -
Molybdenum Cofactor Deficiency: Dietary Therapy
by: J Gordon Millichap
Published: (1993) -
MRI Findings and Outcome in Molybdenum Cofactor Deficiency
by: J Gordon Millichap
Published: (2011) -
A New Pattern of Brain and Cord Gadolinium Enhancement in Molybdenum Cofactor Deficiency: A Case Report
by: Giulia Lucignani, et al.
Published: (2023)