Molecular Cell Biology
Molecular Cell Biology
8th Edition
ISBN: 9781464183393
Author: Harvey Lodish, Arnold Berk, Chris A. Kaiser, Monty Krieger, Anthony Bretscher, Hidde Ploegh, Angelika Amon, Kelsey C. Martin
Publisher: W. H. Freeman
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Chapter 24, Problem 13RTC
Summary Introduction

To write:

The usual signal transduction occurrence which is disturbed by cancer enhancing mutations in the genes that encodes RAS and NF-1.The reason for the mutations in RAS that are generally present in cancers than mutations in NF-1

Introduction:

Neurofibromatosis type 1 or NF1 is an autosomal dominant genetic disorder. Its other name is peripheral neurofibromatosis. It results due to the NF1 gene mutation or deletion. Only a single copy of this modified NF1 gene is enough to affect an individual. It has been well known that neurofibromatosis type 1. It is with an assessed incidence of about 1 in 3,000 individuals.

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