Fine-structure mapping of the hereditary inclusion body myopathy locus

Genomics

Volumn 55, Issue 1, 1999, Pages 43-48

  Eisenberg, Iris ^a   Thiel, Corinna ^c   Levi, Tatjana ^d   Tiram, Efrat ^a   Argov, Zohar ^b   Sadeh, Menachem ^e   Jackson, Cynthia L ^f   Thierfelder, Ludwig ^c   Mitrani Rosenbaum, Stella ^a  

^a HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^b HEBREW UNIVERSITY   (Israel)

^c MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^d HARVARD MEDICAL SCHOOL   (United States)

^e WOLFSON MEDICAL CENTER   (Israel)

^f BROWN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TROPOMYOSIN;

ARTICLE; CELL INCLUSION; CHROMOSOME 9P; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; GENOTYPE; HAPLOTYPE; HUMAN; INCLUSION BODY MYOSITIS; JEW; MALE; MYOPATHY; PRIORITY JOURNAL;

EID: 0032965080     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1998.5630     Document Type: Article

References (17)

1. Argov Z., Yarom R. "Rimmed vacuole myopathy" sparing the quadriceps: A unique disorder in Iranian Jews. J. Neurol. Sci. 64:1984;33-43.
2. Argov Z., Tiram E., Eisenberg I., Sadeh M., Seidman C. E., Seidman J. G., Karpati G., Mitrani-Rosenbaum S. Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1. Ann. Neurol. 41:1997;548-551.
3. Askanas V., Engel W. K. New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathies. Curr. Opin. Rheumatol. 7:1995;486-496.
4. Collins A., Frezal J., Teague J., Morton N. E. A metric map of humans: 23,500 loci in 850 bands. Proc. Natl. Acad. Sci. USA. 93:1996;14771-14775.
5. Harley H. G., Brook J. D., Floyd J., Rundle S. A., Crow S., Walsh K. V., Thibault M-C. Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. Am. J. Hum. Genet. 49:1991;68-75.
6. Hastbacka J., de la Chapelle A., Maahtani M. M., Clines G., Reevee-Daly M. P., Daly M., Hamilton B. A., Kusumi K., Trivedi B., Weaver A., Coloma A., Lovett M., Buckler A., Kaitila I., Lander E. S. The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping. Cell. 78:1994;1073-1087.
7. Ikeuchi T., Asaka T., Saito M., Tanaka H., Higuchi S., Tanaka K., Saida K., Uyama E., Mizusawa H., Fukuhara N., Nonaka I., Takamori M., Tsuji S. Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9. Ann. Neurol. 41:1997;432-437.
8. Jackson C. L., Britt D. E., Graw S. L., Potts A., Santoro K., Buckler A. J., Housman M. H. Construction and characterization of radiation hybrids for chromosome 9 and their use in mapping cosmid probes on the chromosome. Somatic Cell Mol. Genet. 18:1992;285-301.
9. Jorde L. B., Watkins W. S., Carlson M., Groden J., Albertsen H., Thliveras A., Leppert M. Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region. Am. J. Hum. Genet. 54:1994;884-898.
10. Laing N. G., Wilton S. D., Akkari P. A., Dorosz S., Boundy K., Kneebone C., Blumbergs P., White S., Watkins H., Love D. R., Haan E. A mutation in the α tropomyosin gene TMP3 associated with autosomal dominant nemaline myopathy. Nat. Genet. 9:1995;75-79.
11. Lathrop G. M., Lalouel J. M., Julier C., Ott J. Strategies for multilocus linkage analysis in humans. Proc. Natl. Acad. Sci. USA. 81:1984;3443-3446.
12. Lees M. J., Helfman D. M. The molecular basis for tropomyosin isoform diversity. BioEssays. 13:1991;429-437.
13. Mitrani-Rosenbaum S., Argov Z., Blumenfeld A., Seidman C. E., Seidman J. G. Hereditary inclusion body myopathy maps to chromosome 9p1-q1. Hum. Mol. Genet. 5:1996;159-163.
14. Richard I., Broux O., Allamand V., Fougerousse F., Chiannikulchai N., Bourg N., Brenguier L., Devaud C., Pasturaud P., Roudaut C., Hillaire D., Passos-Bueno M-R., Zatz M., Tischfield J. A., Fardeau M., Jackson C. E., Cohen D., Beckmann J. S. Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A. Cell. 81:1995;27-40.
15. Sadeh M., Gadoth M., Hadar H., Ben David E. Vacuolar myopathy sparing the quadriceps. Brain. 16:1993;217-232.
16. Terwilliger J. D. A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. Am. J. Hum. Genet. 56:1995;777-787.
17. Thierfelder L., Watkins H., MacRae C., Lamas R., McKenna W. J., Vosberg H-P., Seidman J. G., Seidman C. E. α tropomyosin and troponin mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere. Cell. 77:1994;701-712.