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As per available reports about 75 Editors, 317 Speakers 73 symposiums are presently dedicated exclusively to Genetic Mutations and about 99 articles are being published on Genetic Mutations.
A gene mutation is a permanent alteration in the DNA sequence that makes up a gene, such that the sequence differs from what is found in most people. Mutations range in size; they can affect anywhere from a single DNA building block (base pair) to a large segment of a chromosome that includes multiple genes.
Mutation plays an important role in evolution. The ultimate source of all genetic variation is mutation. Mutation is important as the first step of evolution because it creates a new DNA sequence for a particular gene, creating a new allele. Genetic Mutations are the key to species evolving. Lets say an organism mutates, there is really only three outcomes.
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Scope & Importance:
To function correctly, each cell depends on thousands of proteins to do their jobs in the right places at the right times. Sometimes, gene mutations prevent one or more of these proteins from working properly. By changing a gene’s instructions for making a protein, a mutation can cause the protein to malfunction or to be missing entirely. When a mutation alters a protein that plays a critical role in the body, it can disrupt normal development or cause a medical condition. A condition caused by mutations in one or more genes is called a genetic disorder.
In some cases, gene mutations are so severe that they prevent an embryo from surviving until birth. These changes occur in genes that are essential for development, and often disrupt the development of an embryo in its earliest stages. Because these mutations have very serious effects, they are incompatible with life.
It is important to note that genes themselves do not cause disease—genetic disorders are caused by mutations that make a gene function improperly. For example, when people say that someone has “the cystic fibrosis gene,” they are usually referring to a mutated version of the CFTR gene, which causes the disease. All people, including those without cystic fibrosis, have a version of the CFTR gene.
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Related Associations & Societies
1. Armenian Society of Human Genetics
2. Austrian Society of Human Genetics
3. Austrian Society of Human Genetics
4. Belgian Society of Human Genetics
5. British Society of Genetic Medicine
6. Bulgarian Society of Human Genetics
Genomic Companies :
2. Genetic Technologies Group
4. Ambry Genetics
5. Biospyder Technologies
6. Predictive biology
8. Cypher Genomics
9. Agena Bioscience
This page will be updated regularly.
This page was last updated on 15th Sep, 2015
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