Muscular dystrophies and protein mutations (2007)
- Authors:
- USP affiliated authors: VAINZOF, MARIZ - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Subjects: DISTROFIA MUSCULAR; DOENÇAS NEUROMUSCULARES; MUTAÇÃO GENÉTICA; PROTEÍNAS MUSCULARES
- Language: Inglês
- Imprenta:
- Publisher: Springer Science
- Publisher place: New York
- Date published: 2007
- ISBN: 978-0-387-36534-3
- Source:
- Título: Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases
- Volume/Número/Paginação/Ano: 538 p
-
ABNT
VAINZOF, Mariz e ZATZ, Mayana. Muscular dystrophies and protein mutations. Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases. Tradução . New York: Springer Science, 2007. . . Acesso em: 26 fev. 2026. -
APA
Vainzof, M., & Zatz, M. (2007). Muscular dystrophies and protein mutations. In Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases. New York: Springer Science. -
NLM
Vainzof M, Zatz M. Muscular dystrophies and protein mutations. In: Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases. New York: Springer Science; 2007. [citado 2026 fev. 26 ] -
Vancouver
Vainzof M, Zatz M. Muscular dystrophies and protein mutations. In: Protein misfolding, aggregation, and conformational diseases. Part B: molecular mechanisms of conformational diseases. New York: Springer Science; 2007. [citado 2026 fev. 26 ] - Um novo locus para uma forma tardia de doença do neurônio motor/esclerose lateral aminotrófica
- Calpainopatia: surpresas nos estudos de correlação genótipo: fenótipo
- Expressão de distrofia em co-culturas de células-tronco de cordão umbilical e mioblastos de pacientes afetados pela DMD
- Characterization of Human Skeletal Muscle Ankrd2
- Partial telethonin deficiency in severely affected North American limb girdle muscular dystrophy patients
- Duchenne clinically discordant brothers: a "Ringo-like" phenotype in humans?
- Partial telethonin deficiency in severely affected north american LGMD patients
- Sarcomeric myopalladin study in limb girdle muscular dystrophies
- Fukutin-related protein gene mutations in brazilian limb-girdle muscular dystrophy families
- GDF-8 expression and the degeneration/regeneration process in mdx mice
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
