Examples of 'due to mutations' in a sentence
Meaning of "due to mutations"
due to mutations: This phrase is used to explain that a change or variation has occurred as a result of mutations in genetic material
How to use "due to mutations" in a sentence
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due to mutations
Familial hyperglycemia due to mutations in glucokinase.
Due to mutations emerged second and third blood group.
Sarcolemmal instability due to mutations in dystrophin has a cascade effect.
The majority of juvenile hemochromatosis cases are due to mutations in hemojuvelin.
They are due to mutations in genes that are involved in making muscle proteins.
Natural variants can occur due to mutations in the proteins.
Pigmentation process maybe affected in one or many ways due to mutations.
In order to investigate structural effects due to mutations structural information is needed.
It is often due to mutations in certain genes involved with making heart muscle proteins.
Certain forms of albinism are known to be due to mutations in tyrosine metabolism.
This is due to mutations in the IGHMBP2 gene.
Polymorphism arises due to mutations.
OCA1 is caused due to mutations in tyrosinase gene affecting its catalytic or synthetic activity.
This phenotype might be due to mutations in the LTR.
Furthermore, the non-resistant varieties did not become resistant due to mutations.
See also
Some mitochondrial diseases are due to mutations or deletions in the mitochondrial genome.
Hereditary hemochromatosis is an autosomal recessive disease and generally due to mutations in HFE gene.
They can be small either due to mutations in the formation of blood cells.
Moreover, different kinds of cancers are also due to mutations.
Human beings born with shorter telomeres due to mutations in their telomerase live shorter lives.
It is due to mutations in the ADA2 gene which encodes the adenosine deaminase 2 protein.
All forms of HSP are due to mutations of various genes.
A proto-oncogene is a normal gene that could become an oncogene due to mutations or increased expression.
Most cases are due to mutations in the ABCA4 gene.
Abstract, Cystic fibrosis is an autosomic recessive disease due to mutations in the gene CFTR.
Abnormal hemoglobins due to mutations in the B-chain are relatively uncommon.
Cystic fibrosis ( CF ) is a genetic disease due to mutations of Cftr gene.
This variation is due to mutations in the FLC and FRIGIDA genes, rendering them non-functional.
There are also many cases of genetic diseases due to mutations in Wnt signaling components.
MEN2 is due to mutations of the RET proto-oncogene.
The most common inherited thrombophilias are due to mutations in the F5 and F2 genes.
This is due to mutations of the CDKN2A and CDK4 genes.
Differences, for example, could be caused due to mutations in the peptides.
The condition is due to mutations in the Wilson disease protein ( " ATP7B " ) gene.
A color variation was seen seen with diploid MFH14 segregants, due to mutations in adenine biosynthesis.
Beta thalassemias are due to mutations in the IIBB gene on chromosome 11.
Abstract, Sandhoff disease ( SD ) is a genetic disorder due to mutations in the HEXB gene.
It originates due to mutations in the ALMS1 gene coding for a protein of 460 kDa.
Differences, for example, could be caused due to mutations in said peptide ( see below ).
They are, of course, due to mutations in the populations.
Voyager selected VY-SOD101 as a clinical candidate for ALS due to mutations in SOD1 gene.
Beta thalassemias are due to mutations in the HBB gene on chromosome 11.
The first one, autosomal recessive, is due to mutations in ADAMTSL2 gene.
Gut dysfunction in autism could be due to mutations that affect neuronal communication . ".
Hereditary breast and ovarian cancer due to mutations in BRCA1 and BRCA2.
Osteogenesis imperfecta causes fragile bones due to mutations in the collagen-I-encoding genes, COLIA1 or COLIA2.
Among the familial cases, approximately 20 % are due to mutations in the SOD1 gene.
Carpenter syndrome is due to mutations in genes RAB23 and MEGF8.
Wolman 's disease is caused due to mutations in the LAL genes.
Leigh syndrome in the mother is due to mutations in the mitochondrial DNA.
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Examples of using Mutations
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These mutations most likely are compensatory mutations
Most loss of function mutations are selected against
