Screening for mutations in the C-terminal region of RYR1 gene identify high frequency of autosomal recessive form of central core disease (CCD) in Brazil

Kossugue, P. M.; Muniz, V. P.; Pavanello, RCM; Silva, H. C.; Giannetti, J. G.; Paim, JFO; Zatz, M.; Vainzof, M.

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/38788

Title:

Screening for mutations in the C-terminal region of RYR1 gene identify high frequency of autosomal recessive form of central core disease (CCD) in Brazil

Author(s):

Institution:

Universidade de São Paulo (USP)
Universidade Estadual Paulista (UNESP)
Universidade Federal de Minas Gerais (UFMG)
RSHAL

ISSN:

0960-8966

Issue Date:

1-Oct-2005

Citation:

Neuromuscular Disorders. Oxford: Pergamon-Elsevier B.V., v. 15, n. 9-10, p. 680-680, 2005.

Time Duration:

680-680

Publisher:

Elsevier B.V.

Source:

http://www.sciencedirect.com/science/article/pii/S0960896605001884

URI:

Access Rights:

Acesso restrito

Type:

outro

Source:

http://repositorio.unesp.br/handle/11449/38788

Artigos, TCCs, Teses e Dissertações da Unesp

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