메뉴 건너뛰기




Volumn 7, Issue 4, 1997, Pages 256-260

Welander distal myopathy is not linked to other defined distal myopathy gene loci

Author keywords

Allelic heterogeneity; Exclusion mapping; Linkage; Welander distal myopathy

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 14Q; CHROMOSOME 2; CLINICAL FEATURE; EXTENSOR MUSCLE; FINLAND; FOOT; GENE LOCUS; GENETIC LINKAGE; GENOME; HAND MUSCLE; HUMAN; MAJOR CLINICAL STUDY; MIYOSHI MYOPATHY; MORPHOLOGY; MYOPATHY; PRIORITY JOURNAL; SWEDEN;

EID: 0030924321     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(97)00451-3     Document Type: Article
Times cited : (12)

References (24)
  • 1
    • 0028951204 scopus 로고
    • Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14
    • Bejaoui K, Hirabayashi K, Hentati F, et al. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Neurology 1995:45:768-72.
    • (1995) Neurology , vol.45 , pp. 768-772
    • Bejaoui, K.1    Hirabayashi, K.2    Hentati, F.3
  • 2
    • 0028813434 scopus 로고
    • Autosomal dominant distal myopathy: Linkage to chromosome 14
    • Laing NG, Laing BA, Meredith C, et al. Autosomal dominant distal myopathy: linkage to chromosome 14. Am J Hum Genet 1995:56:422-7.
    • (1995) Am J Hum Genet , vol.56 , pp. 422-427
    • Laing, N.G.1    Laing, B.A.2    Meredith, C.3
  • 3
    • 0029011231 scopus 로고
    • Distal myopathies. 25th ENMC International workshop
    • 18-20 November 1994, Naarden, The Netherlands
    • Somer H. Distal myopathies. 25th ENMC International workshop. 18-20 November 1994, Naarden, The Netherlands. Neuromusc Disord 1995:5:249-52.
    • (1995) Neuromusc Disord , vol.5 , pp. 249-252
    • Somer, H.1
  • 4
    • 0003132648 scopus 로고
    • Myopathia distalis tarda hereditaria
    • Welander L. Myopathia distalis tarda hereditaria. Acta Med Scand 1951:141:1-124.
    • (1951) Acta Med Scand , vol.141 , pp. 1-124
    • Welander, L.1
  • 5
    • 0018594106 scopus 로고
    • Motor neuron firing range, axonal conduction velocity, and muscle fibre histochemistry in neuromuscular diseases
    • Borg J, Grimby L, Hannerz J. Motor neuron firing range, axonal conduction velocity, and muscle fibre histochemistry in neuromuscular diseases. Muscle Nerve 1979:2:423-30.
    • (1979) Muscle Nerve , vol.2 , pp. 423-430
    • Borg, J.1    Grimby, L.2    Hannerz, J.3
  • 6
    • 0014485677 scopus 로고
    • Signs of neuropathy in distal hereditary myopathy (Welander)
    • Stålberg E, Ekstedt J. Signs of neuropathy in distal hereditary myopathy (Welander). Electroenceph clin Neurophysiol 1969:26:343.
    • (1969) Electroenceph Clin Neurophysiol , vol.26 , pp. 343
    • Stålberg, E.1    Ekstedt, J.2
  • 7
    • 0016763981 scopus 로고
    • Histochemical and histopathological changes in skeletal muscles in late-onset hereditary myopathy (Welander)
    • Edström L. Histochemical and histopathological changes in skeletal muscles in late-onset hereditary myopathy (Welander). J Neurol Sci 1975:26:147-57.
    • (1975) J Neurol Sci , vol.26 , pp. 147-157
    • Edström, L.1
  • 8
    • 0025770238 scopus 로고
    • Welander's distal myopathy: Clinical, neurophysiological and muscle biopsy observations in young and middle-aged adults with early symptoms
    • Borg K, Åhlberg G, Borg J, Edström L. Welander's distal myopathy: clinical, neurophysiological and muscle biopsy observations in young and middle-aged adults with early symptoms. J Neurol Neurosurg Psychiat 1991:54:494-8.
    • (1991) J Neurol Neurosurg Psychiat , vol.54 , pp. 494-498
    • Borg, K.1    Åhlberg, G.2    Borg, J.3    Edström, L.4
  • 9
    • 0024582686 scopus 로고
    • Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reation
    • Weber JL, May PE. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reation. Am J Hum Genet 1989:44:388-96.
    • (1989) Am J Hum Genet , vol.44 , pp. 388-396
    • Weber, J.L.1    May, P.E.2
  • 10
    • 0000926583 scopus 로고
    • Nonradioactive multiplex procedure for genotyping of microsatellite markers
    • Vignal A, Gyapay G, Hazan J, et al. Nonradioactive multiplex procedure for genotyping of microsatellite markers. Methods Mol Genet 1993:211-21.
    • (1993) Methods Mol Genet , pp. 211-221
    • Vignal, A.1    Gyapay, G.2    Hazan, J.3
  • 11
    • 0026446099 scopus 로고
    • A second generation linkage map of the human genome
    • Weissenbach J, Gyapay G, Dib C, et al. A second generation linkage map of the human genome. Nature 1992:359:794-801.
    • (1992) Nature , vol.359 , pp. 794-801
    • Weissenbach, J.1    Gyapay, G.2    Dib, C.3
  • 13
    • 0023205323 scopus 로고
    • Exclusion mapping
    • Edwards JH. Exclusion mapping. J Med Genet 1987:24:539-43.
    • (1987) J Med Genet , vol.24 , pp. 539-543
    • Edwards, J.H.1
  • 15
    • 0022634885 scopus 로고
    • Autosomal recessive distal muscular dystrophy as anew type of progressive muscular dystrophy: Seven cases in eight families, including an autopsied case
    • Miyoshi K, Kawai H, Iwasa M, Kuska K, Nishino H. Autosomal recessive distal muscular dystrophy as anew type of progressive muscular dystrophy: seven cases in eight families, including an autopsied case. Brain 1986:109:31-54.
    • (1986) Brain , vol.109 , pp. 31-54
    • Miyoshi, K.1    Kawai, H.2    Iwasa, M.3    Kuska, K.4    Nishino, H.5
  • 16
    • 0019481203 scopus 로고
    • Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation
    • Nonaka I, Sunohara N, Ishiura S, Satoyosi E. Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation. J Neurol Sci 1981:51:141-55.
    • (1981) J Neurol Sci , vol.51 , pp. 141-155
    • Nonaka, I.1    Sunohara, N.2    Ishiura, S.3    Satoyosi, E.4
  • 17
    • 0027278526 scopus 로고
    • Tibial muscular dystrophy. Late adult onset distal myopathy in 66 Finnish patients
    • Udd B, Partanen J, Halonen P, et al. Tibial muscular dystrophy. Late adult onset distal myopathy in 66 Finnish patients. Arch Neurol 1993:50:604-8.
    • (1993) Arch Neurol , vol.50 , pp. 604-608
    • Udd, B.1    Partanen, J.2    Halonen, P.3
  • 18
    • 0007478851 scopus 로고    scopus 로고
    • Molecular pathology
    • Bios Scientific Publishers
    • Strachan T, Read AP. Molecular pathology. In: Human Molecular Genetics. Bios Scientific Publishers, 1996:401-26.
    • (1996) Human Molecular Genetics , pp. 401-426
    • Strachan, T.1    Read, A.P.2
  • 19
    • 0026741581 scopus 로고
    • Dinucleotide repeat polymorphism at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita
    • D. M-Y
    • McClatchey I, Trofatter J, D. M-Y, et al. Dinucleotide repeat polymorphism at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita. Am J Hum Genet 1992:50:896-901.
    • (1992) Am J Hum Genet , vol.50 , pp. 896-901
    • McClatchey, I.1    Trofatter, J.2
  • 20
    • 0028326542 scopus 로고
    • A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p
    • Bashir R, Strachan T, Keers S, et al. A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p. Hum Mol Genet 1994:3:455-7.
    • (1994) Hum Mol Genet , vol.3 , pp. 455-457
    • Bashir, R.1    Strachan, T.2    Keers, S.3
  • 21
    • 0026690760 scopus 로고
    • Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: Linkage of an autosomal form to chromosome 5q
    • Speer MC, Yamaoka LH, Gilchrist JH, et al. Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal form to chromosome 5q. Am J Hum Genet 1992:50:1211-7.
    • (1992) Am J Hum Genet , vol.50 , pp. 1211-1217
    • Speer, M.C.1    Yamaoka, L.H.2    Gilchrist, J.H.3
  • 22
    • 84965220279 scopus 로고
    • A lecture on myopathy and a distal form
    • Gowers WR. A lecture on myopathy and a distal form. Br Med J 1902:2:89-92.
    • (1902) Br Med J , vol.2 , pp. 89-92
    • Gowers, W.R.1
  • 23
    • 0023832568 scopus 로고
    • Molecular cloning and chromosomal localization of a grene coding for human cardiac myosin heavy chain
    • Matsuoka R, Chambers A, Kimura M, et al. Molecular cloning and chromosomal localization of a grene coding for human cardiac myosin heavy chain. Am J Med Genet 1989:29:369-76.
    • (1989) Am J Med Genet , vol.29 , pp. 369-376
    • Matsuoka, R.1    Chambers, A.2    Kimura, M.3
  • 24
    • 0023197380 scopus 로고
    • Two different forms of beta myosin heavy chain are expressed in human striated muscle
    • Jandreski MA, Sole MJ, Liew C-C. Two different forms of beta myosin heavy chain are expressed in human striated muscle. Hum Genet 1987:77:127-31.
    • (1987) Hum Genet , vol.77 , pp. 127-131
    • Jandreski, M.A.1    Sole, M.J.2    Liew, C.-C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.