Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08NS001591-04
Application #
2259556
Study Section
NST-2 Subcommittee (NST)
Project Start
1993-06-01
Project End
1998-05-31
Budget Start
1996-06-01
Budget End
1997-05-31
Support Year
4
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Iowa
Department
Pediatrics
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Grewal, P K; van Deutekom, J C; Mills, K A et al. (1997) The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8. Mamm Genome 8:394-8
Mills, K A; Ellison, J W; Mathews, K D (1996) The Ant1 gene maps near Klk3 on proximal mouse chromosome 8. Mamm Genome 7:707
Mills, K A; Mathews, K D; Scherpbier-Heddema, T et al. (1996) Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8. Genomics 36:374-6
Mathews, K D; Mills, K A; Bailey, H L et al. (1995) Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q. Muscle Nerve 2:S98-102
Mills, K A; Sunada, Y; Campbell, K P et al. (1995) A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene. Mamm Genome 6:664-5
Mills, K A; Mathews, K D; Scherpbier-Heddema, T et al. (1995) Genetic mapping near the myd locus on mouse chromosome 8. Mamm Genome 6:278-80