Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI) (1998)
- Authors:
- USP affiliated authors: ZATZ, MAYANA - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; MARIE, SUELY KAZUE NAGAHASHI - FM
- Unidades: IB; FM
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Muscle & Nerve
- Volume/Número/Paginação/Ano: suppl. 7, p. 1, 1998
- Conference titles: International Congress on Neuromuscular Diseases
-
ABNT
ZATZ, Mayana et al. Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI). Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 16 abr. 2024. , 1998 -
APA
Zatz, M., Marie, S. K. N., Cerqueira, A., Vainzof, M., Pavanello, R. C. M., & Passos-Bueno, M. R. (1998). Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI). Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo. -
NLM
Zatz M, Marie SKN, Cerqueira A, Vainzof M, Pavanello RCM, Passos-Bueno MR. Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI). Muscle & Nerve. 1998 ; 1.[citado 2024 abr. 16 ] -
Vancouver
Zatz M, Marie SKN, Cerqueira A, Vainzof M, Pavanello RCM, Passos-Bueno MR. Different gender expression and penetrance of the facioscapulohumeral muscular dystrophy gene (FSDHI). Muscle & Nerve. 1998 ; 1.[citado 2024 abr. 16 ] - Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex
- Mecanismo molecular da distrofia muscular fácio-escápulo-humeral: ainda uma incógnita!
- Análise molecular de pacientes brasileiros com ataxia espinocerebelar
- Estudo molecular das neuropatias periféricas hereditárias - CMT1A e HNPP
- Clinical and molecular analysis of spinal muscular atrophy in brazilian patients
- Estudo molecular da neuropatia de Charcot-Marie-Tooth tipo 1 (CMT1) e neuropatia hereditária com paralisias por compressão (HNPP)
- Autosomal dominant pure spastic paraplegia in a brazilian family: linkage to chromosome 8q and study of muscle syntrophin 'beta'1
- A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies
- The FSHD1 gene affects more often and more severely males than females in brazilian families: implications for preclinical and prenatal diagnosis
- Estudo molecular de neuropatias periféricas - CMT1A e HNPP
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
