kiaa1033/washc4

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Novel KIAA1033/WASHC4 mutations in three patients with syndromic intellectual disability and a review of the literature.

Assoum, Mirna;Bruel, Ange-Line;Crenshaw, Melissa L;Delanne, Julian;Wentzensen, Ingrid M;McWalter, Ki...

2020 american journal of medical genetics part a DOI: 10.1002/ajmg.a.61487 242 views

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american journal of medical genetics part a

ISSN: 1552-4833 513 views

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intellectual disability exome sequencing