Cargando…
Vitamin D Status and VDR Genotype in NF1 Patients: A Case-Control Study from Southern Brazil
Neurofibromatosis type 1 (NF1) patients are more likely to have vitamin D deficiency when compared to the general population. This study aimed to determine the levels of 25-OH-vitamin D [25(OH)D] in individuals with NF1 and disease-unaffected controls and analyze FokI and BsmI VDR gene polymorphisms...
Autores principales: | Souza Mario Bueno, Larissa, Rosset, Clévia, Aguiar, Ernestina, Pereira, Fernando de Souza, Izetti Ribeiro, Patrícia, Scalco, Rosana, Matzenbacher Bittar, Camila, Brinckmann Oliveira Netto, Cristina, Gischkow Rucatti, Guilherme, Chies, José Artur, Camey, Suzi Alves, Ashton-Prolla, Patricia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487339/ https://www.ncbi.nlm.nih.gov/pubmed/26161090 http://dx.doi.org/10.1155/2015/402838 |
Ejemplares similares
-
TSC1 and TSC2 gene mutations and their implications
for treatment in Tuberous Sclerosis Complex: a review
por: Rosset, Clévia, et al.
Publicado: (2017) -
BRCA1 and BRCA2 mutational profile and prevalence in hereditary breast and ovarian cancer (HBOC) probands from Southern Brazil: Are international testing criteria appropriate for this specific population?
por: Alemar, Bárbara, et al.
Publicado: (2017) -
Correction: BRCA1 and BRCA2 mutational profile and prevalence in hereditary breast and ovarian cancer (HBOC) probands from Southern Brazil: Are international testing criteria appropriate for this specific population?
por: Alemar, Bárbara, et al.
Publicado: (2018) -
Clinical and molecular characterization of patients fulfilling Chompret criteria for Li-Fraumeni syndrome in Southern Brazil
por: Matzenbacher Bittar, Camila, et al.
Publicado: (2021) -
Systems Biology Approaches Reveal Potential Phenotype-Modifier Genes in Neurofibromatosis Type 1
por: Woycinck Kowalski, Thayne, et al.
Publicado: (2020)