Human Genome Epidemiology Literature Finder
Records 1 - 1 (of 1 Records) |
Query Trace: Myopia and NEUROD1[original query] |
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Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalities. Diabetes 2010 Sep 59 (9): 2326-31. Rubio-Cabezas Oscar, Minton Jayne A L, Kantor Iren, Williams Denise, Ellard Sian, Hattersley Andrew |
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- Page last updated:Mar 18, 2024
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