Overlapping phenotypes in patients harboring heterozygous mutations in KAT6A and KAT6B

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Author(s):	Estrella, S. ; Bertola, D. ; Yamamoto, G. L. ; Honjo, R. ; Ceroni, J. R. ; Kim, C. A. Total Authors: 6
Document type:	Journal article
Source:	European Journal of Human Genetics; v. 27, p. 1-pg., 2019-07-01.

FAPESP's process:	15/21783-9 - Analysis of genetic variants in rare osteochondrodysplasias using whole exome sequencing
Grantee:	Débora Romeo Bertola
Support Opportunities:	Regular Research Grants