Results 241 to 250 of about 762,520 (384)

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

Money and the Morality of Exchange [PDF]

open access: green, 1990
Jay Spaulding   +2 more
openalex   +1 more source

Deciding Morality of Graphs is NP-complete [PDF]

open access: green, 1993
Tikesh Verma, J. Pearl
openalex   +1 more source

UDP‐glucose dehydrogenase variants cause dystroglycanopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
Abstract UDP‐glucose dehydrogenase (UGDH) variants have been associated with hypotonia, developmental delay, and epilepsy. We report the first pathologic evidence of dystroglycanopathy in siblings with UGDH variants. Both presented around 6 months with developmental delay and elevated creatinine kinase.
Anna M. Reelfs   +8 more
wiley   +1 more source

Editorial: Culture and morality: things we value. [PDF]

open access: yesFront Psychol
Wu MS, Ma-Kellams C, Xie T, Zhang Y.
europepmc   +1 more source

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