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De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder.
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has major subject area list
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Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Neurodevelopmental Disorders; Transcription Factor 7-Like 2 Protein
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information resource reference
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Dias C, Pfundt R, Kleefstra T, Shuurs-Hoeijmakers J, Boon EMJ, van Hagen JM, Zwijnenburg P, Weiss MM, Keren B, Mignot C, Isapof A, Weiss K, Hershkovitz T, Iascone M, Maitz S, Feichtinger RG, Kotzot D, Mayr JA, Ben-Omran T, Mahmoud L, Pais LS, Walsh CA, Shashi V, Sullivan JA, Stong N, Lecoquierre F, Guerrot AM, Charollais A, Rodan LH. De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder. Am J Med Genet A. 2021 08; 185(8):2384-2390.
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label
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De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder.
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- Neurodevelopmental Disorder
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