Robert Hufnagel to Atrophy
This is a "connection" page, showing publications Robert Hufnagel has written about Atrophy.
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A de novo hexokinase 1 (HK1) variant presenting as Boucher-Neuh?user syndrome. Am J Med Genet A. 2023 02; 191(2):624-629.
Score: 0.054
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Novel progressive acrodysostosis-like skeletal dysplasia, cerebellar atrophy, and ichthyosis. Am J Med Genet A. 2020 10; 182(10):2214-2221.
Score: 0.046