Hereditary inclusion body myopathy maps to chromosome 9p1-q1

Human Molecular Genetics

Volumn 5, Issue 1, 1996, Pages 159-163

  Mitrani Rosenbaum, Stella ^a,b   Argov, Zohar ^b   Blumenfeld, Anat ^b   Seidman, Christine E ^c   Seidman, J G ^a  

^a HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^b HEBREW UNIVERSITY   (Israel)

^c BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID BETA PROTEIN;

ARTICLE; CELL INCLUSION; CHROMOSOME 9P; CLINICAL ARTICLE; FEMALE; GENE MAPPING; HUMAN; HUMAN CELL; JEW; LIMB GIRDLE MUSCULAR DYSTROPHY; MALE; MYOPATHY; PRIORITY JOURNAL;

ADULT; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GENOTYPE; HUMANS; INCLUSION BODIES; JEWS; LOD SCORE; MALE; MUSCLE WEAKNESS; MUSCULAR DISEASES; PEDIGREE; PERSIA;

ATAXIA;

EID: 0030063986     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.1.159     Document Type: Article

References (24)

1. Mikol, J. and Engel, A.G. (1994) Inclusion body myositis. In Engel, A.G and Franzini-Armstrong C (eds) Myology: Basic and Clinical McGraw-Hill, New York, pp. 1384-1398.
2. Sekul, E.A. and Dalakas, M.C. (1993) Inclusion body myositis. new concepts. Seminars in Neurol., 13: 256-263.
3. Askanas, V. and Engel, W.K. (1993) New advances in inclusion body myositis. Curr. Opinion Rheumatology, 5: 732-741.
4. Askanas, V., Engel, W.K., Bilak, M., Alvarez, R.B. and Selkoe, D J. (1994) Twisted tubofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau. Am. J. Pathol. 144: 177-187.
5. Argov, Z. and Yarom, R. (1984) 'Rimmed vacuole myopathy' sparing the quadriceps: a unique disorder in Iranian Jews. J. Neurol. Sci., 64: 33-43
6. Sadeh, M., Gadoth, M., Hadar, H. and Ben David, E. (1993) Vacuolar myopathy sparing the quadriceps. Brain, 16: 217-232.
7. Massa, R., Weller, B., Karpati, G., Shoubridge, E. and Carpenter, S. (1991) Familial inclusion body Myositis among Kurdish-Iranian Jews. Arch Neurol., 48: 519-522.
8. Mendell, J.R., Sahenk, Z , Gales, T. and Paul, L. (1991) Amyloid filaments in inclusion body myositis. Arch. Neurol., 48: 1229-1234.
9. Fujita R., Hanauer, A., Vincent, A., Mandel, J.-L. and Koenig, M. (1991) Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresis Genomics, 10: 915-920.
10. Carvajal, J.J., Pook, M.A., Doudney, K., Hillermann, R., Wilkes, D., Al-Mahdawi, S., Williamson, R. and Chamberlain, S. (1995) Friedreich's ataxia: a defect in signal transduction? Hum. Mol. Genet., 4: 1411-1419.
11. Criggs, R. and Mendell, J. (1995) Summary of workshop on sporadic and familial inclusion body myopathy. Ann. Neurol., in press.
12. Neufeld, M.Y., Sadeh, M., Assa, B., Kushnir, M. and Korczyn, A.D. (1995) Phenotypic heterogeneity in familial inclusion body myopathy. Muscle & Nerve, 18: 546-548
13. Pollak, M.R., Chou, Y.H., Cerda, J.J., Steinmann, B., La Du, B.N., Seidman J.G. and Seidman C.E. (1993) Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2. Nature Genet., 5: 201-204.
14. Gyapay, G., Morissette, J , Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M. and Weissenbach J. (1994) The 1993-1994 Genethon human genetic linkage map. Nature Genet., 7: 246-339.
15. Povey, S., Armour J., Farndon, P., Haines, J. L., Knowles M., Olopade, F., Pilz, A., White, J.A., members of the Utah Genome Center Genetic Marker and Mapping Group and Kwiatkowski, D. J. (1994) Report on the third international workshop on chromosome 9. Ann. Hum. Genet., 58: 177-250.
16. Collins, A., Forabosco, P., Lawrence, S. and Morton, N. (1995) An integrated map of chromosome 9. Ann. Hum. Genet., in press.
17. Netzer, A. (1988) The Jewish communities in Iran. In Iranian Jews, Koresh House-World Center of Iranian Jews in Israel, Tel Aviv, pp. 3-20.
18. Sivakumar, K. and Dalakas, M.C. (1995) Quadriceps sparing (qs) myopathy: an autosomal recessive, early onset, familial inclusion body myopathy (F-IBM) in non Iranian-Jewish families. Neurology, 45 (suppl.4): 209.
19. Neville, H.E., Baumbach, L.L., Ringel, S.P., Russo, L.S., Sujansky, E. and Garcia, C.A., (1992) Familial inclusion body myositis: evidence for autosomal dominant inheritance. Neurology, 42: 897-902.
20. Cole, A.J., Kuzniecky, R.R., Karpati, G., Carpenter, S., Andermann, E. and Andermann F. (1988) Familial myopathy with changes resembling inclusion body myositis and periventricular leucoencephalopathy. Brain, 11: 1025-1037.
21. Fardeau, M., Askanas, V., Tome, F.M.S., Engel, W.K., Alvarez, R., McFerrin, J. and Chevallay, M. (1990) Hereditary neuromuscular disorders with inclusion body myositis-like filamentous inclusions: clinical, pathological and tissue culture studies. Neurology, 40 (suppl. 1): 120.
22. Kligman, J.G., Gibbs, M.A. and Creek, W. (1991) Familial inclusion body myositis. Neurology, 41 (suppl. 1): 275.
23. Richards, E.J. (1992) Preparation and analysis of DNA. In Ausubel, R.M. et al.(eds) Current Protocols in Molecular Biology, Green Publishing, New York, 2.0.1-2.9.11.
24. Lathrop, G.M., Lalouel, J.M., Julier, C. and Ott, J. (1984) Strategies for multilocus linkage analysis in humans. Proc. Natl. Acad. Sci. U.S.A., 81: 3443-3446.