Correlation of DNA expansion and systemic manifestations in myotonic dystrophy (1997)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; ZATZ, MAYANA - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidades: FM; IB
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of the Neurological Sciences
- Volume/Número/Paginação/Ano: v. 150, n. suppl, p. S324, 1997
- Conference titles: World Congress of Neurology
-
ABNT
TEIXEIRA, V. G et al. Correlation of DNA expansion and systemic manifestations in myotonic dystrophy. Journal of the Neurological Sciences. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 19 set. 2024. , 1997 -
APA
Teixeira, V. G., Zatz, M., Marie, S. K. N., Passos-Bueno, M. R., & Reed, U. C. (1997). Correlation of DNA expansion and systemic manifestations in myotonic dystrophy. Journal of the Neurological Sciences. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Teixeira VG, Zatz M, Marie SKN, Passos-Bueno MR, Reed UC. Correlation of DNA expansion and systemic manifestations in myotonic dystrophy. Journal of the Neurological Sciences. 1997 ; 150( suppl): S324.[citado 2024 set. 19 ] -
Vancouver
Teixeira VG, Zatz M, Marie SKN, Passos-Bueno MR, Reed UC. Correlation of DNA expansion and systemic manifestations in myotonic dystrophy. Journal of the Neurological Sciences. 1997 ; 150( suppl): S324.[citado 2024 set. 19 ] - Molecular analysis of spinal muscular atrophy in brazilian patients
- Deficiency of 'alfa'-actinin-3 (ACTN3) Occurs in different forms of muscular dystrophy
- Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations
- Deficiencia de merosina na distrofia muscular congenita associada a alteracao da substancia branca cerebral
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
- Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- Associacao do retardo mental com delecoes dos exons 50 a 54 do gene da distrofina em pacientes com distrofia muscular tipo duchenne
- Estudos de ligação em famílias com ataxia espinocerebelar
- Localizacao de genes responsaveis pelas distrofias musculares tipo cinturas atraves de microsatelites
- Different mosaicism frequencies for proximal and distal duchenne muscular dystrophy (dmd) mutations indicate difference in etiology and recurrence risk
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