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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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SENP7-Related Fatal Arthrogryposis Multiplex Congenita and Immunodeficiency: A Novel Missense Variation and Syndromic
Pratima Pal1, Gayatri Nerakh2, Shreya Bhat1
1Clinical Genomics & Bioinformatics Services, AIC-CCMB, Hyderabad, India.
Abstract:
of prominent clinical features and molecular findings of SENP7-associated disorder in previous cases and our case.
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