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NG1802
NG1802
http://dx.doi.org/10.1038/NG1802
Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism.
P356
Q48087598-18C115A1-3388-4C88-A546-5E5180BED9F4
P356
NG1802
http://dx.doi.org/10.1038/NG1802