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UnknownThe association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease.
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S-EPMC6382903 | biostudies-literature
UnknownUnique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome.
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S-EPMC7784914 | biostudies-literature
UnknownCC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow.
Not available
S-EPMC11339347 | biostudies-literature
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