Results 231 to 240 of about 1,984,825 (269)

Identification of an elusive <i>SERPING1</i> deletion in a family with hereditary angioedema type I utilizing soft clipping. [PDF]

open access: yesFront Allergy
Wetherby K   +8 more
europepmc   +1 more source

Mitochondrial DNA disorders in neuromuscular diseases in diverse populations

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao   +34 more
wiley   +1 more source

DNA content, repeatome composition and origin of the Zea mays micronuclei. [PDF]

open access: yesSci Rep
Tostes NV   +5 more
europepmc   +1 more source

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