Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1

Annals of Neurology

Volumn 41, Issue 4, 1997, Pages 548-551

  Argov, Zohar ^a   Tiram, Efrat ^b   Eisenberg, Iris ^b   Sadeh, Menahem ^c   Seidman, Christine E ^d   Seidman, J G ^d   Karpati, George ^e   Mitrani Rosenbaum, Stella ^b  

^a HEBREW UNIVERSITY   (Israel)

^b HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^c SHEBA MEDICAL CENTER   (Israel)

^d HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^e MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CELL VACUOLE; CHROMOSOME 9; FEMALE; GENE LOCUS; HUMAN; HUMAN CELL; INCLUSION BODY MYOPATHY; INCLUSION BODY MYOSITIS; MAJOR CLINICAL STUDY; MALE; MUSCLE WEAKNESS; PRIORITY JOURNAL;

ADULT; AFGHANISTAN; CANADA; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; DNA; FEMALE; FRANCE; HUMANS; IRAQ; ISRAEL; JEWS; LINKAGE (GENETICS); LOD SCORE; MALE; MYOSITIS, INCLUSION BODY; PEDIGREE;

EID: 0030929664     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410410419     Document Type: Article

References (17)

1. Mikol J, Engel AG. Inclusion body myositis. In: Engel AG, Franzini-Armstrong C, eds. Myology. 2nd ed. New York: McGraw-Hill, 1994:1384-1398
2. Criggs RC, Askanas V, DiMauro S, et al. Inclusion body myositis and myopathies. Ann Neurol 1995;38:705-715
3. Askanas V, Engel WK. New advances in inclusion body myosicis. Curr Opin Rheumatol 1993;5:732-741
4. Figarella-Branger D, Pellissier JF, Bianco N, et al. Inflammatory and non inflammatory inclusion body myositis. Acta Pathol 1990;79:528-536
5. Argov Z, Yarom R. "Rimmed vacuole myopathy" sparing the quadriceps: a unique disorder in Iranian Jews. J Neurol Sci 1984;64:33-43
6. Sadeh M, Gadoth M, Hadar H, Ben David E. Vacuolar myopathy sparing the quadriceps. Brain 1993;16:217-232
7. Massa R, Weller B, Karpati G, et al. Familial inclusion body myositis among Kurdish-Iranian Jews. Arch Neurol 1991;48: 519-522
8. Sadeh M, Argov Z. Hereditary inclusion body myopathy in Jews of Persian origin: clinical and laboratory data. In: Askanas V, Serratrice G, eds. Inclusion body myositis. New York: Cambridge Press, 1997 (in press)
9. Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, et al. Hereditary inclusion body myopathy maps to chromosome 9pl-ql. Hum Mol Genet 1996;5:159-163
10. Cole AJ, Kuzniecky RR, Karpati G, et al. Familial myopathy with changes resembling inclusion body myositis and periventricular leucoencephalopathy. Brain 1988;11:1025-1037
11. Gyapay G, Morissette J, Vignal A, et al. The 1993-1994 Genethon human genetic linkage map. Nat Genet 1994;7:246-339
12. Rodius F, Duclos F, Wrogemann K, et al. Recombinations in individuals homozygous by descent localize ehe Friedreich Ataxia locus in a cloned 450kb interval. Am J Hum Genet 1994;54:1050-1059
13. Neufeld MY, Sadeh M, Assa B, et al. Phenotypic heterogeneity in familial inclusion body myopathy. Muscle Nerve 1995;18: 546-548
14. Argov Z, Mitrani-Rosenbaum S. Hereditary inclusion body myopathy (H-IBM) with quadriceps sparing: epidemiology and genetics. In: Askanas V, Serratrice G, eds. Inclusion body myositis. New York: Cambridge Press, 1997 (in press)
15. Sivakumar K, Dalakas MC. Quadriceps sparing (qs) myopathy: an autosomal recessive, early onset, familial inclusion body myopathy (F-IBM) in non Iranian-Jewish families. Neurology 1995;45(suppl 4):209-213
16. Hentati F, Ben Hamida C, Tome F, et al. Familial inclusion body myositis sparing the quadriceps with asymptomatic leukoencephalopathy in a Tunisian kindred. Neurology 1991;41(suppl 1):422
17. Nonaka I, Sunohara N, Ishiura S, Satayoshi E. Familial distal myopathy with rimmed vacuoles and lamellar (myeloid) body formation. J Neurol Sci 1981;51:l41-145