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.
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A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report.Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl.The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome
P2860
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.
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2017年の論文
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name
Sanger sequencing in exonic re ...... e report of a Chinese patient.
@en
Sanger sequencing in exonic re ...... ovel de-novo germline mutation
@nl
type
label
Sanger sequencing in exonic re ...... e report of a Chinese patient.
@en
Sanger sequencing in exonic re ...... ovel de-novo germline mutation
@nl
prefLabel
Sanger sequencing in exonic re ...... e report of a Chinese patient.
@en
Sanger sequencing in exonic re ...... ovel de-novo germline mutation
@nl
P2093
P2860
P1433
P1476
Sanger sequencing in exonic re ...... se report of a Chinese patient
@en
P2093
Bai-Rong Li
Shu-Han Sun
Xiao-Wei Jin
Yu-Liang Jiang
P2860
P2888
P356
10.1186/S12881-017-0471-Y
P577
2017-11-15T00:00:00Z
P6179
1092693145