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: 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: 11 fev. 2026. , 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 2026 fev. 11 ] -
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 2026 fev. 11 ] - Um novo locus para uma forma tardia de doença do neurônio motor/esclerose lateral aminotrófica
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