Homozygosity Facial Features
Sept. 10, 2024
ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9 | Nature Communications Clinical findings of an individual with a homozygous missense GINS2... | Download Scientific Diagram Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome | Journal of Medical Genetics Homozygosity Facial Features
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