Associated Papers
Case report: Whole exome sequencing identified a novel mutation (p.Y301H) of MAF in a Chinese family with congenital cataracts.
Lin ZJ et al.
Frontiers in Medicine, 2024
Functional and In Silico Assessment of GDF3 Gene Variants in a Chinese Congenital Scoliosis Population.
Chen J et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2018
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