<scp>SHP2</scp> 's gain‐of‐function in <scp>Werner</scp> syndrome causes childhood disease onset likely resulting from negative genetic interaction-Reference-Cited by-同舟云学术

SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction

Published:2022-04-17 Issue:1 Volume:102 Page:12-21
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Priolo Manuela¹,Palermo Valentina²,Aiello Francesca²,Ciolfi Andrea³,Pannone Luca³⁴,Muto Valentina³,Motta Marialetizia³,Mancini Cecilia³,Radio Francesca Clementina³^ORCID,Niceta Marcello³^ORCID,Leoni Chiara⁵^ORCID,Pintomalli Letizia¹,Carrozzo Rosalba³^ORCID,Rajola Giuseppe⁶,Mammì Corrado¹,Zampino Giuseppe⁵,Martinelli Simone⁴,Dallapiccola Bruno³,Pichierri Pietro²,Tartaglia Marco³^ORCID

Affiliation:

1. Genetica Medica, Grande Ospedale Metropolitano "Bianchi Melacrino Morelli" Reggio Calabria Italy

2. Department of Environment and Health Mechanisms Istituto Superiore di Sanità Rome Italy

3. Genetics and Rare Diseases Research Division Ospedale Pediatrico Bambino Gesù, IRCCS Rome Italy

4. Department of Oncology and Molecular Medicine Istituto Superiore di Sanità Rome Italy

5. Center for Rare Disease and Congenital Defects, Fondazione Policlinico Universitario A. Gemelli Università Cattolica del Sacro Cuore Rome Italy

6. UOC Pediatria, Azienda Ospedaliera “Pugliese‐Ciaccio” Catanzaro Italy

Funder

Associazione Italiana per la Ricerca sul Cancro

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14140

Reference51 articles.

1. Positional Cloning of the Werner's Syndrome Gene

2. The spectrum ofWRNmutations in Werner syndrome patients

3. Spectrum and Risk of Neoplasia in Werner Syndrome: A Systematic Review

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