Chapter 15 Brain Tumors and the Lynch Syndrome
Lynch syndrome (LS) (MIM No. 120435-6), previously known as hereditary nonpolyposis colorectal cancer (HNPCC) (Boland, 2005), is an autosomal dominant disorder caused by germline mutation in one of the DNA mismatch repair (MMR) genes. LS is among the most prevalent cancer syndromes in man and is e...
में बचाया:
मुख्य लेखक: | Peltomäki, Päivi (auth) |
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अन्य लेखक: | Gylling, Annette (auth) |
स्वरूप: | इलेक्ट्रोनिक पुस्तक अध्याय |
भाषा: | अंग्रेज़ी |
प्रकाशित: |
InTechOpen
2011
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विषय: | |
ऑनलाइन पहुंच: | DOAB: download the publication DOAB: description of the publication |
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समान संसाधन
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Chapter 15 Brain Tumors and the Lynch Syndrome
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