Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: ATP6V0C[original query] |
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A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Sep . Mucha Bettina E, Banka Siddharth, Ajeawung Norbert Fonya, Molidperee Sirinart, Chen Gary G, Koenig Mary Kay, Adejumo Rhamat B, Till Marianne, Harbord Michael, Perrier Renee, Lemyre Emmanuelle, Boucher Renee-Myriam, Skotko Brian G, Waxler Jessica L, Thomas Mary Ann, Hodge Jennelle C, Gecz Jozef, Nicholl Jillian, McGregor Lesley, Linden Tobias, Sisodiya Sanjay M, Sanlaville Damien, Cheung Sau W, Ernst Carl, Campeau Philippe |
PFKFB2 Promoter Hypomethylation as Recurrence Predictive Marker in Well-Differentiated Thyroid Carcinomas. International journal of molecular sciences 2019 3 20 (6): . Camargo Barros-Filho Mateus, Barreto Menezes de Lima Larissa, Bisarro Dos Reis Mariana, Bette Homem de Mello Julia, Moraes Beltrami Caroline, Lopes Pinto Clóvis Antonio, Kowalski Luiz Paulo, Rogatto Silvia Regi |
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