Kennedy's disease: A clinicopathologic correlation with mutations in the androgen receptor gene

Neurology

Volumn 43, Issue 4, 1993, Pages 791-794

  Amato, A A ^a   Prior, T W ^a   Barohn, R J ^b   Snyder, P ^a   Papp, A ^a   Mendell, J R ^a  

^a OHIO STATE UNIVERSITY   (United States)

^b UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR; DNA;

ADULT; AGED; ALLELE; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE SEVERITY; EXON; FRAGILE X SYNDROME; GENE MUTATION; HEREDITARY SPINAL MUSCULAR ATROPHY; HETEROZYGOTE DETECTION; HUMAN; MALE; MYOTONIC DYSTROPHY; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; X CHROMOSOME RECESSIVE INHERITANCE;

COMPARATIVE STUDY; CREATINE KINASE; DNA; FEMALE; FRAGILE X SYNDROME; HETEROZYGOTE; HUMAN; LINKAGE (GENETICS); MALE; MUSCLES; MUSCULAR ATROPHY; MUSCULAR ATROPHY, SPINAL; MUTATION; MYOTONIC DYSTROPHY; NECROSIS; PEDIGREE; PHENOTYPE; RECEPTORS, ANDROGEN; SURAL NERVE; X CHROMOSOME;

EID: 0027503515     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/wnl.43.4.791     Document Type: Article

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