Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two brazilians siblings

Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two brazilians siblings (2017)

Authors:
USP affiliated authors: MARTELLI, LUCIA REGINA - FMRP
Unidades: FMRP
Subjects: MUTAÇÃO GENÉTICA; FENÓTIPOS
Language: Inglês
Imprenta:
- Publisher: FMRP-USP
- Place of publication: Ribeirão Preto
- Date published: 2017
Source:
- Título do periódico: Resumos
Conference title: Workshop do Programa de Pós-Graduação em Genética da FMRP-USP

A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

ABNT

GRANGEIRO, C. H. P.; HUBER, Jair; MARTELLI, Lúcia Regina. Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two brazilians siblings. Anais.. Ribeirão Preto: FMRP-USP, 2017.
APA

Grangeiro, C. H. P., Huber, J., & Martelli, L. R. (2017). Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two brazilians siblings. In Resumos. Ribeirão Preto: FMRP-USP.
NLM

Grangeiro CHP, Huber J, Martelli LR. Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two brazilians siblings. Resumos. 2017 ;
Vancouver

Grangeiro CHP, Huber J, Martelli LR. Asparagine synthetase deficiency detected by whole exome sequencing: the first description in two brazilians siblings. Resumos. 2017 ;