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"Disease genetics" » "Disease genetic" (Expand Search)
Showing 1 - 4 results of 4 for search '"Disease genetics"', query time: 0.02s Refine Results
  1. 1
    Biallelic <i> </i><i>NAA60</i> variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications

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

    Published 2024
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  2. 2
    Bi-allelic truncating variants in <i>CASP2</i> underlie a neurodevelopmental disorder with lissencephaly

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

    Published 2023
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  3. 3
    Effect of ALOX5AP gene variants on coronary artery disease risk. (c2009)

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

    Published 2009
    Subjects: “…Coronary heart disease -- Genetic aspects…”
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  4. 4
    Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants

    Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants by Amal Elfatih (14778550)

    Published 2024
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