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SETBP1 gene variants: from Schinzel-Giedion syndrome to mild neurodevelopmental disorder, a challenge for the clinician
SETBP1 gene variants: from Schinzel-Giedion syndrome to mild neurodevelopmental disorder, a challenge for the clinician
2020
A. Moroni
Diana Carli
E Giorgio
Fabio Sirchia
Lisa Pavinato
S. Cardaropoli
P Di Martino
Alessandro Mussa
T. Pipucci
S De Rubeis
Alfredo Brusco
Keywords:
SETBP1 Gene
Pediatrics
Schinzel–Giedion syndrome
Neurodevelopmental disorder
Medicine
Correction
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