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In the remaining one-third of cases, a gene on another chromosome is responsible for the disease, and two copies of the defective gene, one from each parent, must be inherited for the disease to arise (a type of inheritance called autosomal recessive).
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This procedure allows us to define parametric controls and cases for any type of inheritance mode (H) and selection coefficient (s).
Lastly, this genetic element offers an example of a type of Lamarckian inheritance in prokaryotes (Koonin and Wolf 2009).
While it is only logical to raise the estate tax threshold to a modern-day level, repealing the tax for all types of inheritance ignores its valuable purpose.
Besides being the only mutation with an autosomal dominant type of inheritance reported thus far, the Ogna mutation is emerging as the most frequent mutation of plectin described in families of different ethnic origins, suggesting that it may represent a hotspot for mutations within the plectin gene.
The equal protection clause of the 14th Amendment should not be extended to all types of inheritance (letter, Dec. 27).
In this case, the clams that were examined exhibit an exceptional and interesting type of inheritance pattern of their mitochondrial genomes called doubly uniparental.
Stratification on the basis of type of inheritance showed the prevalence among inherited widows ranging from a low of 54.8% in widows who were inherited by a relative primarily for companionship to a high of 73.8% in widows who were inherited by a non-relative primarily for sexual ritual.
In this type of inheritance pattern, each offspring of an affected individual has a 50% risk of inheriting the mutant allele and therefore being affected with the disorder (see figure).
The second type of inheritance strategy is an ordered process in which organelles are actively delivered by the cytoskeleton into daughter cells.
POLG mutations can, therefore, lead to a spectrum of mitochondrial diseases with dominant or recessive type of inheritance, which can be divided into three main groups: sporadic/familial progressive external ophthalmoplegia (PEO) (OMIM #157640 and #258450), adult-onset ataxia (OMIM #607459), and Alpers syndrome (OMIM #203700).
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