becker muscular dystrophy造句

Such mutations are associated with the much milder Becker muscular dystrophy.
The genetic mutation that leads to Becker muscular dystrophy is an in-frame deletion.
Mutations in Myf-6 can provoke disorders including centronuclear myopathy and Becker muscular dystrophy.
There is no known cure for Becker muscular dystrophy yet.
Worton and his team identified the dystrophin gene whose mutation is associated with Becker muscular dystrophies.
It's difficult to find becker muscular dystrophy in a sentence. 用becker muscular dystrophy造句挺难的

Additionally, in Duchenne muscular dystrophy and Becker muscular dystrophy, the expression of alpha-7B integrin was enhanced.
The Duchenne and Becker muscular dystrophy.
His doctoral research led to his landmark discovery of the gene responsible for X-linked Duchenne and Becker muscular dystrophy.
This truncated dystrophin protein produced by eteplirsen causes a less severe form of dystrophinopathy, much like Becker muscular dystrophy.
Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients.
Biostrophin is a delivery vector for gene therapy in the treatment of Duchenne muscular dystrophy and Becker muscular dystrophy.
"' Biostrophin "'is a drug which may serve as a vehicle for gene therapy, in the treatment of Becker muscular dystrophy.
In 1961 Dreifuss and colleagues described a family with form of muscular dystrophy distinct from more severe Duchenne and Becker muscular dystrophies.
Becker muscular dystrophy occurs in approximately 1.5 to 6 in 100, 000 male births, making it much less common than Duchenne muscular dystrophy.
Men who have Becker muscular dystrophy can have children, and all their daughters are carriers, but none of the sons will inherit their father's mutation.

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