Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I (2011)
- Authors:
- Autor USP: MARQUES JÚNIOR, WILSON - FMRP
- Unidade: FMRP
- Subjects: DOENÇAS DO SISTEMA NERVOSO; GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of The Peripheral Nervous System
- ISSN: 1085-9489
- Volume/Número/Paginação/Ano: v. 16, suppl. 3, p. S14-S15, 2011
- Conference titles: Meeting of The Peripheral Nerve Society
-
ABNT
BUENO, K. C. et al. Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I. Journal of The Peripheral Nervous System. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 2011 -
APA
Bueno, K. C., Gouvêa, S. P., Lourenço, C. M., & Marques Júnior, W. (2011). Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I. Journal of The Peripheral Nervous System. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Bueno KC, Gouvêa SP, Lourenço CM, Marques Júnior W. Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I. Journal of The Peripheral Nervous System. 2011 ; 16 S14-S15.[citado 2024 out. 17 ] -
Vancouver
Bueno KC, Gouvêa SP, Lourenço CM, Marques Júnior W. Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I. Journal of The Peripheral Nervous System. 2011 ; 16 S14-S15.[citado 2024 out. 17 ] - Identification of five novel mutations in brazilian families with X-linked CMT
- Male monozygotic twins discordant for periventricular nodular heterotopia and epilepsy
- Análise da qualidade de vida de pacientes com a doença de Charcot-Marie-Tooth tipo 1a
- Does pregnancy change the natural history of CMT1A neuropathy?
- The genetic landscape of axonal neuropathies in the middle-aged and elderly
- A heterozygous PMP22 THR(118)MET substitution running in a family with 17PTANDEM duplication
- Sensory neuronopathy III-electromyography
- Estudo comparativo da condução sensitivo-motora do nervo ulnar em pacientes com neuropatia hereditária com sensibilidade à compressão e com neuropatia do mal de Hansen
- Spinocerebellar ataxia type 7: clinical features in brazilian family
- Association of two dominant autosomal disorders in the same family: AEC7 and CMT1A
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas