David Dyment
0000-0001-9085-3602
3 papers found
Refreshing results…
Enhanced cGAS-STING–dependent interferon signaling associated with mutations in ATAD3A
Whole genome sequencing reveals biallelic PLA2G6 mutations in siblings with cerebellar atrophy and cap myopathy
Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants
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