Associated Papers
CYP26B1-related disorder: expanding the ends of the spectrum through clinical and molecular evidence.
Silveira KC et al.
Human Genetics, 2023
Characterizing rare and low-frequency height-associated variants in the Japanese population.
Akiyama M et al.
Nature Communications, 2019
Mucopolysaccharidosis IIIB and mild skeletal anomalies: coexistence of NAGLU and CYP26B1 missense variations in the same patient in a Chinese family.
Li J et al.
Bmc Medical Genetics, 2018
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