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Science (New York, N.Y.)|November 16, 1990
Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit geneB Fontaine, T S Khurana, E P Hoffman, et al.
Human Genetics|November 1, 1994
Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21P Gregor, S M Gaston, X Yang, et al.
Journal of Special Operations Medicine : a Peer Reviewed Journal for SOF Medical Professionals|December 16, 2022
Experience With Trauma-Induced ARDS: A Retrospective Study of US Wartime Casualties 2003-2015Jason J Nam, Matthew S McCravy, Krista L Haines, et al.
Annals of Neurology|November 1, 1990
A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
American Journal of Ophthalmology|December 7, 2007
Phenotype analysis of patients with the risk variant LOC387715 (A69S) in age-related macular degenerationR Keith Shuler, Silke Schmidt, Paul Gallins, et al.
Journal of the Neurological Sciences|July 1, 1994
Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21D A Figlewicz, M G McInnis, J Goto, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Neovascular age-related macular degeneration and its association with LOC387715 and complement factor H polymorphismR Keith Shuler, Michael A Hauser, Jennifer Caldwell, et al.
Carcinogenesis|April 24, 2007
Genetic variation in TP53 and risk of breast cancer in a population-based case control studyBrian L Sprague, Amy Trentham-Dietz, Montserrat Garcia-Closas, et al.
American Journal of Medical Genetics|July 13, 2001
Evidence supporting WNT2 as an autism susceptibility geneT H Wassink, J Piven, V J Vieland, et al.
Cell|March 2, 1992
Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenitaA I McClatchey, P Van den Bergh, M A Pericak-Vance, et al.
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