Refined localization of the human α-tropomyosin gene (TPM1) by genetic mapping

Cytogenetics and Cell Genetics

Volumn 84, Issue 1-2, 1999, Pages 35-36

  Mogensen, Jens ^a   Kruse, T A ^b   Borglum A D ^b  

^a AARHUS UNIVERSITY HOSPITAL   (Denmark)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

TROPOMYOSIN;

ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FREQUENCY; GENE LOCATION; GENE MAPPING; GENETIC LINKAGE; HUMAN; HUMAN CELL; HYPERTROPHIC CARDIOMYOPATHY; MEDICAL GENETICS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

CARDIOMYOPATHY, HYPERTROPHIC; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; GENETIC MARKERS; HUMANS; LINKAGE (GENETICS); LOD SCORE; TROPOMYOSIN;

EID: 0032944758     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

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6. Tiso N, Rampoldi L, Pallavicini A, Zimbello R, Pandolfo D, Valle G, Lanfranchi G, Danieli GA: Fine mapping of five human skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow-twitch, troponin-I fast-twitch, and troponin-C fast. Biochem biophys Res Commun 230:347-350 (1997).