Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype

被引：10

作者：

Segui, Nuria ^{[1
]}

Navarro, Matilde ^{[1
]}

Pineda, Marta ^{[1
]}

Koeger, Nicole ^{[2
]}

Bellido, Fernando ^{[1
]}

Gonzalez, Sara ^{[1
]}

Campos, Olga ^{[1
]}

Iglesias, Silvia ^{[1
]}

Valdes-Mas, Rafael ^{[3
]}

Lopez-Doriga, Adriana ^{[4
,5
]}

Gut, Marta ^{[6
]}

Blanco, Ignacio ^{[1
]}

Lazaro, Conxi ^{[1
]}

Capella, Gabriel ^{[1
]}

Puente, Xose S. ^{[3
]}

Plotz, Guido ^{[2
]}

Valle, Laura ^{[1
]}

机构：

[1] IDIBELL, Hereditary Canc Program, Catalan Inst Oncol, Lhospitalet De Llobregat 08908, Spain

[2] Univ Klinikum Frankfurt, Med Klin 1, Biomed Res Lab, D-60590 Frankfurt, Germany

[3] Univ Oviedo, Dept Biochem & Mol Biol, Inst Univ Oncol, Oviedo, Spain

[4] IDIBELL, Catalan Inst Oncol, Unit Biomarkers & Susceptibil, Lhospitalet De Llobregat, Spain

[5] CIBERESP, Lhospitalet De Llobregat, Spain

[6] Fundacio Parc Cient Barcelona, Ctr Nacl Anal Genom, Barcelona, Spain

来源：

GUT | 2015年 / 64卷 / 02期

关键词：

POLYPOSIS; GENE;

D O I：

10.1136/gutjnl-2014-307084

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

[No abstract available]

引用

页码：355 / U187

页数：2

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