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Analysis of current testing practices for biallelic MUTYH mutations in MUTYH -associated polyposis

✍ Scribed by Landon, M.; Ceulemans, S.; Saraiya, D.S.; Strike, B.; Arnell, C.; Burbidge, L.A.; Moyes, K.; Theisen, A.; Fernandes, P.H.; Ji, J.Q.; Abbott, B.; Kaldate, R.R.; Roa, B.


Book ID
121685422
Publisher
John Wiley and Sons
Year
2014
Tongue
English
Weight
249 KB
Volume
87
Category
Article
ISSN
0009-9163

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## Abstract To determine the frequency, mutation spectrum and phenotype of the recently described autosomal recessive __MUTYH__‐associated polyposis (MAP), we performed a systematic search for __MUTYH (MYH__) mutations by sequencing the complete coding region of the gene in 329 unselected __APC__ m