Partial telethonin deficiency in severely affected north american LGMD patients (2002)
- Authors:
- USP affiliated authors: ZATZ, MAYANA - IB ; VAINZOF, MARIZ - IB
- Unidade: IB
- Subjects: MUTAÇÃO GENÉTICA; DISTROFIA MUSCULAR; DOENÇAS NEUROMUSCULARES
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of the Neurological Sciences
- Volume/Número/Paginação/Ano: v. 199, supl., p. S58, 2002
- Conference titles: International Congress on Neuromuscular Diseases
-
ABNT
HOUSTON, Ronnie et al. Partial telethonin deficiency in severely affected north american LGMD patients. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 2002 -
APA
Houston, R., Muirhead, D., Elmonoufy, N., Cornelia, R., Faulkner, G., Valle, G., et al. (2002). Partial telethonin deficiency in severely affected north american LGMD patients. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. -
NLM
Houston R, Muirhead D, Elmonoufy N, Cornelia R, Faulkner G, Valle G, Zatz M, Vainzof M, Iannaccone S. Partial telethonin deficiency in severely affected north american LGMD patients. Journal of the Neurological Sciences. 2002 ; 199 S58.[citado 2024 abr. 24 ] -
Vancouver
Houston R, Muirhead D, Elmonoufy N, Cornelia R, Faulkner G, Valle G, Zatz M, Vainzof M, Iannaccone S. Partial telethonin deficiency in severely affected north american LGMD patients. Journal of the Neurological Sciences. 2002 ; 199 S58.[citado 2024 abr. 24 ] - Protein defects in neuromuscular diseases
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