OXFORD, England, Dec. 17 -- Human Molecular Genetics, a peer-reviewed journal that says it features human molecular genetic disease mechanisms from the analysis of mutated genes and disease susceptibility through to therapeutics, published research articles on the following topics in its Jan. 1, 2022 edition:

ARTICLES:

* Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2

* Functional assessment of two variants of unknown signific . . .

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