SCOPUS 정보 검색 플랫폼

Volumn 59, Issue 5, 1996, Pages 1040-1047

Mild and severe muscular dystrophy caused by a single γ-sarcoglycan mutation

(11) McNally, Elizabeth M b Passos Bueno, Maria Rita b Bönnemann, Carsten G b Vainzof, Mariz b De Moreira, Eloisa Sá b Lidov, Hart G W b Othmane, Kamel Ben b Denton, Peter H b Vance, Jeffery M b Zatz, Mayana b Kunkel, Louis M a

a BOSTON CHILDREN S HOSPITAL (United States)

b NONE

Author keywords

[No Author keywords available]

Indexed keywords

GLYCAN DERIVATIVE;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; DISEASE SEVERITY; GENE MUTATION; HUMAN; HUMAN TISSUE; MUSCULAR DYSTROPHY; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ADOLESCENT; ADULT; AFRICA, NORTHERN; BRAZIL; CHILD; CYTOSKELETAL PROTEINS; FEMALE; HUMANS; MALE; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; MUSCULAR DYSTROPHIES; PEDIGREE; POINT MUTATION; POLYMORPHISM, GENETIC; SARCOGLYCANS;

EID: 19244363787 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (150)

References (5)

1
- 0020606260
- Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia
- Ben Hamida M, Fardeau M, Attia N (1983) Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia. Muscle Nerve 6:469-480
- (1983) Muscle Nerve , vol.6 , pp. 469-480
- Ben Hamida, M.¹ Fardeau, M.² Attia, N.³

2
- 0027032694
- Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q
- Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, et al (1992) Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nat Genet 2:315-317
- (1992) Nat Genet , vol.2 , pp. 315-317
- Ben Othmane, K.¹ Ben Hamida, M.² Pericak-Vance, M.A.³ Ben Hamida, C.⁴ Blel, S.⁵ Carter, S.C.⁶ Bowcock, A.M.⁷

3
- 0029152259
- Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)
- Ben Othmane K, Speer MC, Stauffer J, Blel S, Middleton L, Ben Hamida C, Etribi A, et al (1995) Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C). Am J Hum Genet 57:732-734
- (1995) Am J Hum Genet , vol.57 , pp. 732-734
- Ben Othmane, K.¹ Speer, M.C.² Stauffer, J.³ Blel, S.⁴ Middleton, L.⁵ Ben Hamida, C.⁶ Etribi, A.⁷

4
- 0028971219
- β-Sarcoglycan mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
- Bönnemann CG, Modi R, Noguchi S, Mizuno Y, Yoshida M, Gussoni E, McNally EM, et al (1995) β-Sarcoglycan mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex. Nat Genet 11:266-273
- (1995) Nat Genet , vol.11 , pp. 266-273
- Bönnemann, C.G.¹ Modi, R.² Noguchi, S.³ Mizuno, Y.⁴ Yoshida, M.⁵ Gussoni, E.⁶ McNally, E.M.⁷

5
- 0029334512
- The limb girdle muscular dystrophies: Proposal for a new nomenclature
- Bushby KM, Beckmann JS (1995) The limb girdle muscular dystrophies: proposal for a new nomenclature. Neuromuscul Disord 4:337-343
- (1995) Neuromuscul Disord , vol.4 , pp. 337-343
- Bushby, K.M.¹ Beckmann, J.S.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.