| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5905159 | Gene | 2016 | 5 Pages |
Abstract
According to clinical information, whole-exome sequencing results and Sanger verification results, ARHGAP4 (T491M) mutation may be disease-causing gene of the MR patient. The relation between ARHGAP4 mutation and MR clinical characteristic is needed to be illuminated with participation of more MR patients.
Keywords
NDILM-PCRBWAPhytohemagglutininSNPsSIFTXLMRPHAElectroencephalogramMRIintelligence quotientMagnetic resonance imagingSanger sequencingWhole-exome sequencingNephrogenic diabetes insipidusX-linked mental retardationfluorescence in situ hybridizationFishSorting Intolerant From TolerantX-linkedEEGIndelsLigation-mediated polymerase chain reactionSingle nucleotide polymorphismsKaryotypingMental retardation
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Authors
Fuhua Liu, Hui Guo, Minglin Ou, Xianliang Hou, Guoping Sun, Weiwei Gong, Huanyun Jing, Qiupei Tan, Wen Xue, Yong Dai, Weiguo Sui,