Associated Papers
Delayed-Onset NOG Gene-Related Syndromic Conductive Deafness: A Case Report.
Sun H et al.
Ear, Nose, & Throat Journal, 2021
Identification of an unknown frameshift variant of NOG in a Han Chinese family with proximal symphalangism.
Yuan ZZ et al.
Bioscience Reports, 2020
Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.
Ma C et al.
Bmc Medical Genetics, 2019
A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder.
Takano K et al.
Human Genome Variation, 2016
A mutation in the heparin-binding site of noggin as a novel mechanism of proximal symphalangism and conductive hearing loss.
Masuda S et al.
Biochemical and Biophysical Research Communications, 2014
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