SANMATI CUDDAPAH to Neurodevelopmental Disorders
This is a "connection" page, showing publications SANMATI CUDDAPAH has written about Neurodevelopmental Disorders.
Connection Strength
0.218
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Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia. Am J Hum Genet. 2021 12 02; 108(12):2368-2384.
Score: 0.113
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De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females. Genet Med. 2021 04; 23(4):645-652.
Score: 0.105