Looking for one more autosomal recessive limb girdle muscular dystrophy gene (2002)
- Authors:
- USP affiliated authors: VAINZOF, MARIZ - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Subjects: DISTROFIA MUSCULAR; DOENÇAS NEUROMUSCULARES
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of the Neurological Sciences
- Volume/Número/Paginação/Ano: v. 199, supl., p. S57, 2002
- Conference titles: International Congress on Neuromuscular Diseases
-
ABNT
STARLING, A. et al. Looking for one more autosomal recessive limb girdle muscular dystrophy gene. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 28 abr. 2024. , 2002 -
APA
Starling, A., Vainzof, M., Canovas, M., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (2002). Looking for one more autosomal recessive limb girdle muscular dystrophy gene. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. -
NLM
Starling A, Vainzof M, Canovas M, Pavanello R de CM, Passos-Bueno MR, Zatz M. Looking for one more autosomal recessive limb girdle muscular dystrophy gene. Journal of the Neurological Sciences. 2002 ; 199 S57.[citado 2024 abr. 28 ] -
Vancouver
Starling A, Vainzof M, Canovas M, Pavanello R de CM, Passos-Bueno MR, Zatz M. Looking for one more autosomal recessive limb girdle muscular dystrophy gene. Journal of the Neurological Sciences. 2002 ; 199 S57.[citado 2024 abr. 28 ] - Severe Nonspecific X-Linked Mental Retardation Caused by a-Proximally Xp Located Gene: intragenic Heterogeneity or a New Form of X-Linked Mental Retardation?
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