The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies (2000)
- Authors:
- Vainzof, Mariz - Universidade de São Paulo (USP)
- Moreira, E. S. - Universidade de São Paulo (USP)
- Passos-Bueno, Maria Rita
- Faulkner, Georgine
- Valle, G.
- Zanoteli, Edmar - Universidade Federal de São Paulo (UNIFESP)
- Gurgel-Gianneti, Juliana - Universidade de São Paulo (USP)
- Ribeiro, Alberto de Freitas
- Silva, Helga Cristina Almeida da - Universidade de São Paulo (USP)
- Tsanaclis, Ana Maria Crous
- Zatz, Mayana
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB ; RIBEIRO, ALBERTO AUGUSTO G DE F CASTRO - IB ; TSANACLIS, ANA MARIA CROUS - FM
- Unidades: IB; FM
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: The American Journal of Human Genetics
- Volume/Número/Paginação/Ano: v. 67, n. 4, suppl. 2, p. 379, outubro de 2000
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
VAINZOF, Mariz et al. The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies. The American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 2000 -
APA
Vainzof, M., Moreira, E. S., Passos-Bueno, M. R., Faulkner, G., Valle, G., Zanoteli, E., et al. (2000). The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies. The American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. -
NLM
Vainzof M, Moreira ES, Passos-Bueno MR, Faulkner G, Valle G, Zanoteli E, Gurgel-Gianneti J, Ribeiro A de F, Silva HCA da, Tsanaclis AMC, Zatz M. The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies. The American Journal of Human Genetics. 2000 ; 67( 4): 379.[citado 2024 abr. 24 ] -
Vancouver
Vainzof M, Moreira ES, Passos-Bueno MR, Faulkner G, Valle G, Zanoteli E, Gurgel-Gianneti J, Ribeiro A de F, Silva HCA da, Tsanaclis AMC, Zatz M. The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies. The American Journal of Human Genetics. 2000 ; 67( 4): 379.[citado 2024 abr. 24 ] - Caracterização da proteína teletonina na distrofia muscular das cinturas tipo 2G (DMC-2G) e estudo de sua expressão nas outras formas de miopatias
- Caracterização da proteína teletonina na distrofia muscular das cinturas tipo 2G (DMC-2G) e estudo de sua expressão nas outras formas de miopatias
- Sarcolemmal distribution of abnormal dystrophin in xp21 carriers
- Telethonin protein expression in neuromuscular disorders
- Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of duchenne's and becker muscular dystrophies of different ages
- Miopatia de central core e hipertermia maligna: triagem de mutações no gene RYR1 e CACLN1A3
- Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in brazilian families
- Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas