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Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals.

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Bibliographic Details
Title: Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals.
Authors: Owen, Ceris I.1, Bowden, Ramsay2, Parker, Michael J.3, Patterson, Jo3, Patterson, Joan2, Price, Sue4, Sarkar, Ajoy5, Castle, Bruce6, Deshpande, Charulatha7, Splitt, Miranda8, Ghali, Neeti9, Dean, John10, Green, Andrew J.11, Crosby, Charlene12, Deciphering Developmental Disorders Study13, Tatton‐Brown, Katrina12,14, k.tattonbrown@nhs.net
Source: American Journal of Medical Genetics. Part A; May2018, Vol. 176 Issue 5, p1108-1114, 7p
Database: Applied Science & Technology Source
Description
ISSN:15524825
DOI:10.1002/ajmg.a.38610