Examples of 'gene cause' in a sentence
Meaning of "gene cause"
This phrase suggests the role or influence of genes in the development or occurrence of a specific trait, characteristic, or condition. It implies that genetic factors are responsible for the cause or origin of a particular genetic attribute or issue
How to use "gene cause" in a sentence
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gene cause
Defects in this gene cause cystic fibrosis.
This is particularly relevant when large numbers of mutations within a single gene cause a disease pathology.
Some mutations in a gene cause few or no problems.
Single gene cause of insulin sensitivity may offer insight for treating diabetes.
Mutations in this gene cause vitiligo.
Mutations in this gene cause familial Alzheimer 's type 3 with certainty and usually under 50 years old.
Mutations in the PRNP gene cause prion disease.
Mutations in the gene cause a group of syndromes known as ectodermal dysplasias.
Fragile X syndrome is the most common known single gene cause of autism.
How mutations in the gene cause disease is not yet clear.
Fragile X syndrome is the most prevalent known single gene cause of ASD.
Some mutations in the gene cause people to feel more pain.
Indeed, Fragile X Syndrome is the most common known single gene cause of autism.
Mutations in this gene cause the syndrome of apparent mineralocorticoid excess and hypertension.
Certain mutations in the MECP2 gene cause Rett syndrome.
See also
Mutations in the GALC gene cause a deficiency of an enzyme called galactosylceramidase.
Autosomal recessive mutations in the SPTAN1 gene cause a new form of HSP.
Some defects in this same gene cause a condition called oculocutaneous albinism in humans.
Gene alterations ( mutations ) in the PAH gene cause PKU.
Mutations in this gene cause Alstrom syndrome.
Mutations in this gene cause one form of autosomal recessive early-onset Parkinson 's disease.
Mutations in the NOTCH3 gene cause CADASIL.
Mutations in the FGFR1 gene cause a small percentage of cases of type 1 Pfeiffer syndrome.
Gain-of-function mutations in the phosphatidylserine synthase 1 ( PTDSS1 ) gene cause Lenz-Majewski syndrome.
Mutations in the GBA gene cause very low levels of glucocerebrosidase.
Mutations in the ABCA12 gene cause the disease.
Mutations of the NF2 gene cause a human autosomal dominant disease called neurofibromatosis type 2.
Mutations or deletions of a part of the PHEX gene cause X-linked hypophosphatemia ( XLH ).
Defects in the PAX6 gene cause aniridia-like ocular defects in mice as well as Drosophila.
Mutations in the LDL receptor gene cause familial hypercholesterolemia.
Errors in this gene cause glycogen storage disease type II ( Pompe disease ).
Mutations in the PPOX gene cause variegate porphyria.
Mutations associated with this gene cause the most frequent form of autosomal dominant spastic paraplegia 4.
Mutations in the PHEX gene cause this disease.
Mutations in the PANK2 gene cause pantothenate kinase-associated neurodegeneration.
Mutations in the FKRP ( fukutin-relatedprotein ) gene cause a wide range ofphenotypic variability.
Mutations in this gene cause autosomal recessive non-syndromic deafness . [ 1 ].
Mutations in the NDP gene cause Norrie disease.
Mutations in this gene cause X-linked dyskeratosis congenita.
Mutations in the HRAS gene cause Costello syndrome.
Mutations in this gene cause Rubinstein-Taybi syndrome RTS.
Incidentally, mutations in this gene cause the most common form of albinism.
Mutations in the FGD1 gene cause some cases of Aarskog-Scott syndrome.
In general, defects in more than one gene cause each clinical type of ichthyosis.
Mutations in the SLC26A2 gene cause recessive multiple epiphyseal dysplasia.
In these families, mutations in the tau gene cause neuronal cell death and dementia.
Mutations in the Senataxin gene cause ALS4, a juvenile-onset form that usually begins before age 25.
Mutations in the BTD gene cause biotinidase deficiency.
Mutations in the ATM gene cause ataxia-telangiectasia.
Changes in the NF1 gene cause this disease.
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