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CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women

✍ Scribed by Dank, Muriel A. (author);Jonker, Marianne A. (author);Kluijt, Irma (author);van Mil, Saskia E. (author);Oldenburg, Rogier A. (author);Mooi, Wolter J. (author);Hogervorst, Frans B.L. (author);van den Ouweland, Ans M.W. (author);Gille, Johan J.P. (author);Schmidt, Marjanka K. (author);van der Vaart, Aad W. (author);Meijers-Heijboer, Hanne (author);Waisfisz, Quinten (author)

Book ID: 126877379
Publisher: BMJ Publishing Group
Year: 2011
Tongue: English
Weight: 295 KB
Volume: 48
Category: Article
ISSN: 0022-2593
DOI: 10.1136/jmedgenet-2011-100380

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The association between the CHEK2 and breast cancer risk in Chinese women is unknown. Here, we screened the full CHEK2 coding sequence in 118 Chinese familial breast cancer cases who are negative for mutations in BRCA1 and BRCA2, one recurrent mutation, CHEK2 c.1111C4T (p.H371Y), was identified in f