You should search up the info on these chromosomes:
chromosome 1
chromosome 14
chromosome 21
there is also other genes:
presenilin 1 (PS1 or PSEN1)
presenilin 2 (PS2 or PSEN2)
amyloid precursor protein (APP)
There is no "epilepsy gene". The mechanism's for inherited epilepsy are complicated and unknown.
because the Chromosomes get wet by cells with tiny tails with one head and a tail coming from it. that causes it to epilepsy
alzheimers is a gene disorder it is located on chromosome 19 on gene APOE
Click on the link below.
Mutation is caused when chunks of chromosomes cut taken or fall off. So the chromosome with the DNA causes a mutation which sometimes is helpful but mosty hard to live with.
The specific location of the mutation that causes X-ALD is on the ABCD1 gene on the X-chromosome. Please note that there isn't a specific mutation in the ABCD1 gene that causes X-ALD or can be related in any way to the different clinical presentations of the disease.
mutations
choromosome mutaion
Inversion is caused by a) radiation causing the chromosome to break or b) two chromosomes entangling causing one to break. source yahoo answers
An Inversion mutation is a mutation that causes a reversal in the order of a segment of a chromosome within the chromosome, or a gene.
mutation
Mutation is caused when chunks of chromosomes cut taken or fall off. So the chromosome with the DNA causes a mutation which sometimes is helpful but mosty hard to live with.
The permanent change in a gene or a chromosome is called Mutation.
An extra copy of Chromosome 18
A change in a gene or chromosome is called a: Mutation
non-disjunction
The specific location of the mutation that causes X-ALD is on the ABCD1 gene on the X-chromosome. Please note that there isn't a specific mutation in the ABCD1 gene that causes X-ALD or can be related in any way to the different clinical presentations of the disease.
Chromosomal mutation
mutations
Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).
caused by a mutation in a gene called myelin protein zero (MPZ) located on chromosome 1.