## 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
✦ LIBER ✦
MUTYH-associated polyposis – variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations
✍ Scribed by M Morak; A Laner; U Bacher; C Keiling; E Holinski-Feder
- Book ID
- 110889084
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 647 KB
- Volume
- 78
- Category
- Article
- ISSN
- 0009-9163
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