Extending the clinical phenotype associated with biallelic NTHL1 germline mutations-Reference-Cited by-同舟云学术

Extending the clinical phenotype associated with biallelic NTHL1 germline mutations

Published:2018-09-24 Issue:6 Volume:94 Page:588-589
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Fostira Florentia¹^ORCID,Kontopodis Emmanouil²,Apostolou Paraskevi¹^ORCID,Fragkaki Maria²,Androulakis Nikolaos²,Yannoukakos Drakoulis¹,Konstantopoulou Irene¹,Saloustros Emmanouil³

Affiliation:

1. NCSR “Demokritos” Athens Greece

2. General Hospital of Heraklion “Venizelio‐Pananio” Heraklion Greece

3. University of Thessaly Larissa Greece

Funder

State Scholarships Foundation

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13444

Reference4 articles.

1. A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer

2. Biallelic NTHL1 Mutations in a Woman with Multiple Primary Tumors

3. Delineating the Phenotypic Spectrum of the NTHL1-Associated Polyposis

4. NTHL1andMUTYHpolyposis syndromes: two sides of the same coin?

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