Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.

Name: Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.
Author: Zhao, Zi-Ye

Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient. — المؤلف: Zhao, Zi-Ye — BMC medical genetics 20171129

المؤلف: Zhao, Zi-Ye
النشر: BMC medical genetics 20171129
الوصف: 130 p.
الموضوعات: AMP-Activated Protein Kinase Kinases؛ Amino Acid Sequence؛ Asian People؛ China؛ Exons؛ Frameshift Mutation؛ Germ-Line Mutation؛ Humans