Nonketotic hyperglycinemia: Functional assessment of missense variants in GLDC to understand phenotypes of the disease.
第一作者:
Irene,Bravo-Alonso
第一单位:
Centro de Diagnóstico de Enfermedades Moleculares, Centro de Biología Molecular Severo Ochoa, CBM-CSIC, Departamento de Biología Molecular, Universidad Autónoma Madrid, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), IDIPAZ, Madrid, Spain.
作者:
医学主题词
外显子(Exons);基因表达调控, 酶学(Gene Expression Regulation, Enzymologic);甘氨酸(Glycine);甘氨酸脱氢酶(脱羧作用)(Glycine Dehydrogenase (Decarboxylating));人类(Humans);高甘氨酸血症, 非酮性(Hyperglycinemia, Nonketotic);婴儿, 新生(Infant, Newborn);分子构象(Molecular Conformation);突变, 误义(Mutation, Missense);表型(Phenotype);蛋白质稳定性(Protein Stability);构效关系(Structure-Activity Relationship)
DOI
10.1002/humu.23208
PMID
28244183
发布时间
2018-06-28
- 浏览25
Human mutation
678-691页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文


换一批



