Biallelic <i> </i><i>NAA60</i> variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications حسب Viorica Chelban (4569337)

الموضوعات:

Bi-allelic truncating variants in <i>CASP2</i> underlie a neurodevelopmental disorder with lissencephaly حسب Eyyup Uctepe (19342522)

الموضوعات:

Effect of ALOX5AP gene variants on coronary artery disease risk. (c2009) حسب Alwan, Ahmad A.

الموضوعات: "…Coronary heart disease -- Genetic aspects…"
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Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants حسب Amal Elfatih (14778550)

الموضوعات: