Cargando…
Detection of congenital generalized lipodystrophy mutations by next-generation sequencing: time for a new approach
Autores principales: | Riquetto, Aline Dantas Costa, de Santana, Lucas Santos, Caetano, Lílian Araújo, Lerário, Antônio Marcondes, Correia-Deur, Joya Emilie Menezes, Nery, Márcia, de Lima Jorge, Alexander Augusto, Teles, Milena Gurgel |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659283/ http://dx.doi.org/10.1186/1758-5996-7-S1-A260 |
Ejemplares similares
-
Targeted massively parallel sequencing for congenital generalized lipodystrophy
por: Costa-Riquetto, Aline D., et al.
Publicado: (2020) -
Next-generation sequencing in Brazilian MODY patients: a pilot study
por: Caetano, Lílian Araújo, et al.
Publicado: (2015) -
MODY screening: a new center for molecular genetic diagnosis in Brazil
por: de Santana, Lucas Santos, et al.
Publicado: (2015) -
Hypercalcitoninemia is not Pathognomonic of Medullary Thyroid Carcinoma
por: Toledo, Sergio PA, et al.
Publicado: (2009) -
The performance of the MODY calculator in a non-Caucasian, mixed-race population diagnosed with diabetes mellitus before 35 years of age
por: Santomauro, Augusto Cezar, et al.
Publicado: (2023)