SCOPUS 정보 검색 플랫폼

Neuromuscular Disorders

Volumn 18, Issue 12, 2008, Pages 1005-

TPM2 mutation

(3) Brandis, Almuth a Aronica, Eleonora b Goebel, Hans H c

a HANNOVER MEDICAL SCHOOL (Germany)

b ACADEMIC MEDICAL CENTER (Netherlands)

c JOHANNES GUTENBERG UNIVERSITY (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BETA TROPOMYOSIN GENE; ELECTRON MICROSCOPY; GENE; GENE MUTATION; IMMUNOHISTOCHEMISTRY; LETTER; MORPHOLOGY; MUSCLE BIOPSY; NEMALINE MYOPATHY; NEUROMUSCULAR DISEASE; PATHOLOGY; PRIORITY JOURNAL;

BIOPSY; FEMALE; HUMANS; MALE; MUSCLE FIBERS, SKELETAL; MUSCLE FIBERS, SLOW-TWITCH; MUTATION; MYOPATHIES, STRUCTURAL, CONGENITAL; TROPOMYOSIN;

EID: 56749107246 PISSN: 09608966 EISSN: None Source Type: Journal
DOI: 10.1016/j.nmd.2008.07.007 Document Type: Letter

Times cited : (26)

References (5)

1
- 0036133714
- Mutations in the β-tropomyosin (TPM2) gene - a rare cause of nemaline myopathy
- Donner K., Ollikainen M., Ridanpää M., Christen H.J., Goebel H.H., de Visser M., et al. Mutations in the β-tropomyosin (TPM2) gene - a rare cause of nemaline myopathy. Neuromuscul Disord 12 (2002) 151-158
- (2002) Neuromuscul Disord , vol.12 , pp. 151-158
- Donner, K.¹ Ollikainen, M.² Ridanpää, M.³ Christen, H.J.⁴ Goebel, H.H.⁵ de Visser, M.⁶

2
- 34249049197
- Cap disease caused by heterozygous mutation of the beta-tropomyosin gene TPM2
- Lehtokari V.-.L., Ceuterick-de Groote C., de Jonghe P., Martilla M., Laing N.G., Pelin K., et al. Cap disease caused by heterozygous mutation of the beta-tropomyosin gene TPM2. Neuromuscul Disord 17 (2007) 433-442
- (2007) Neuromuscul Disord , vol.17 , pp. 433-442
- Lehtokari, V.-.L.¹ Ceuterick-de Groote, C.² de Jonghe, P.³ Martilla, M.⁴ Laing, N.G.⁵ Pelin, K.⁶

3
- 34447502553
- The pathogenesis of ACTA1-related congenital fiber type disproportion
- Clarke N.F., Ilkovski B., Cooper S., Valova V.A., Robinson P.J., Nonaka I., et al. The pathogenesis of ACTA1-related congenital fiber type disproportion. Ann Neurol 61 (2007) 552-561
- (2007) Ann Neurol , vol.61 , pp. 552-561
- Clarke, N.F.¹ Ilkovski, B.² Cooper, S.³ Valova, V.A.⁴ Robinson, P.J.⁵ Nonaka, I.⁶

4
- 33644819072
- SEPN1: associated with congenital fiber-type disproportion and insulin resistance
- Clarke N.F., Kidson W., Quijano-Roy S., Estournet B., Ferreiro A., Guicheney P., et al. SEPN1: associated with congenital fiber-type disproportion and insulin resistance. Ann Neurol 59 (2006) 546-552
- (2006) Ann Neurol , vol.59 , pp. 546-552
- Clarke, N.F.¹ Kidson, W.² Quijano-Roy, S.³ Estournet, B.⁴ Ferreiro, A.⁵ Guicheney, P.⁶

5
- 27644471429
- A novel X-linked form of congenital fiber-type disproportion
- Clarke N.F., Smith R.L., Bahlo M., and North K.N. A novel X-linked form of congenital fiber-type disproportion. Ann Neurol 58 (2005) 767-772
- (2005) Ann Neurol , vol.58 , pp. 767-772
- Clarke, N.F.¹ Smith, R.L.² Bahlo, M.³ North, K.N.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.