Mining the genome for susceptibility to complex neurological disorders

Current Molecular Medicine

Volumn 9, Issue 7, 2009, Pages 801-813

  Gubitz, A K ^a   Gwinn, K ^b  

^a NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; AMYOTROPHIC LATERAL SCLEROSIS; GENE IDENTIFICATION; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENOME; HUMAN; LINKAGE ANALYSIS; MULTIPLE SCLEROSIS; NEUROLOGIC DISEASE; PARKINSON DISEASE; PATHOGENESIS; PHENOTYPE; PROGRESSIVE SUPRANUCLEAR PALSY; RESTLESS LEGS SYNDROME; REVIEW; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM;

ALZHEIMER DISEASE; AMYOTROPHIC LATERAL SCLEROSIS; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HUMANS; LINKAGE (GENETICS); MULTIPLE SCLEROSIS; NERVOUS SYSTEM DISEASES; PARKINSON DISEASE; RESTLESS LEGS SYNDROME; SUPRANUCLEAR PALSY, PROGRESSIVE;

EID: 70350537423     PISSN: 15665240     EISSN: None     Source Type: Journal    
DOI: 10.2174/156652409789105534     Document Type: Review

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