LOXL3 novel mutation causing a rare form of...

Clinical Genetics 2018 / 10

LOXL3 novel mutation causing a rare form of autosomal recessive Stickler syndrome

Chan, Tin K., Al Kaabi, Mohamed K., ElBarky, Ahmed M., El-Hattab, Ayman W.
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Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.13465
Date:
October, 2018
File:
PDF, 3.70 MB
english, 2018
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