Molecular diagnosis of myotonic dystrophy and Huntington's disease from Calcutta, India

Neurology India

Volumn 46, Issue 3, 1998, Pages 199-203

  Basu, P ^a   Gunguly, P K ^a   Basu, D ^a   Bhattacharyya, N P ^a  

^a SAHA INSTITUTE OF NUCLEAR PHYSICS   (India)

Author keywords

CAG CTG repeat expansion; Huntington's disease; Indian population; Myotonic dystrophy

Indexed keywords

DNA; HUNTINGTIN; MYOTONIC DYSTROPHY PROTEIN KINASE; PROTEIN KINASE; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC SCREENING; HETEROZYGOSITY; HUMAN; HUNTINGTON CHOREA; INDIA; MALE; MOLECULAR GENETICS; MYOTONIC DYSTROPHY; POLYMERASE CHAIN REACTION; TRINUCLEOTIDE REPEAT;

EID: 0032456119     PISSN: 00283886     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (17)