换一批Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth's short tail mouse.
第一作者：
Nirmala,Gurung
第一单位：
Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, Bonn D‑53127, Germany.
作者：
医学主题词
肛管(Anal Canal);动物(Animals);肛门闭锁(Anus, Imperforate);食管(Esophagus);女(雌)性(Female);胎儿(Fetus);心脏缺损, 先天性(Heart Defects, Congenital);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);人类(Humans);肾(Kidney);肢畸形, 先天性(Limb Deformities, Congenital);小鼠(Mice);突变(Mutation);神经管缺损(Neural Tube Defects);妊娠(Pregnancy);桡骨(Radius);脊柱(Spine);气管(Trachea);转录因子(Transcription Factors)
DOI
10.3892/mmr.2015.3486
PMID
25775927
发布时间
2015-04-15
- 浏览0
Molecular medicine reports
1579-83页
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