Mutation screening of acid alpha-1,4-glucosidase gene in 64 patients from latin american (2010)
- Authors:
- USP affiliated authors: Shinjo - ; SHINJO, SUELI MIEKO OBA - FM ; MARIE, SUELY KAZUE NAGAHASHI - FM
- Unidade: FM
- Subjects: MUTAÇÃO GENÉTICA; GENES (ANÁLISE;ENZIMOLOGIA); RASTREAMENTO; MIOCARDIOPATIAS; GENÔMICA; DNA (ANÁLISE); GENÓTIPOS; FENÓTIPOS; RESUMOS (EVENTOS); AMÉRICA LATINA
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP"
-
ABNT
SILVA, R et al. Mutation screening of acid alpha-1,4-glucosidase gene in 64 patients from latin american. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 28 dez. 2025. , 2010 -
APA
Silva, R., Shinjo, S. M. O., Andrade, F. G., & Marie, S. K. N. (2010). Mutation screening of acid alpha-1,4-glucosidase gene in 64 patients from latin american. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Silva R, Shinjo SMO, Andrade FG, Marie SKN. Mutation screening of acid alpha-1,4-glucosidase gene in 64 patients from latin american. Clinics. 2010 ; 65 S75.[citado 2025 dez. 28 ] -
Vancouver
Silva R, Shinjo SMO, Andrade FG, Marie SKN. Mutation screening of acid alpha-1,4-glucosidase gene in 64 patients from latin american. Clinics. 2010 ; 65 S75.[citado 2025 dez. 28 ] - Effect of atorvastatin on muscle tissues of dermatomyositis and antisynthetase syndrome patients with dyslipidemia
- Transcriptional response to GAA deficiency (Pompe disease) in infantile-onset patients
- Significant association between PTPN11 polymorphism and gastric atrophy among japanese brazilians
- Community-based familial study of Helicobacter pylori infection among healthy japaneses brazilians
- Exomic sequencing of four rare central nervous system tumor types
- Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study
- Homozugotic intronic GAA mutation in three siblings with late-onset Pompe's disease
- Role of melkin astrocytoma
- Interleukin 13 receptor alpha 2 (IL13RA2) gene and protein expressions profile in human
- Aberrant expression in astrocytomas of genes envolved in placenta
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
