Article

Unexpected DMD Gene Mutations Detected by CMA and CNV-seq in amniotic Fluid and Aborted Fetus Samples

2021-04-05

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are common X chromosome-linked recessive hereditary diseases. The mechanism is that the exon mutations of anti-myatrophy protein gene (Dystrophin gene) and lead to muscle dysfunction. Prenatal diagnosis can prevent the birth of children with defects and have good clinical significance. <bold>M...

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Literature Corpus work: 0d993af3-1368-54cd-9125-13dd97bab570
DOI: 10.21203/rs.3.rs-376139/v1

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Unexpected DMD Gene Mutations Detected by CMA and CNV-seq in amniotic Fluid and Aborted Fetus SamplesDOI 10.21203/rs.3.rs-376139/v1Read

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