Associated Papers
Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity.
Liu KY et al.
Orphanet Journal of Rare Diseases, 2018
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.
Hwang DY et al.
Human Genetics, 2015
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