Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies-Reference-Cited by-同舟云学术

Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies

Published:2019-01 Issue:1 Volume:104 Page:94-111
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Khan Tahir N.,Khan Kamal,Sadeghpour Azita,Reynolds Hannah,Perilla Yezmin,McDonald Marie T.,Gallentine William B.,Baig Shahid M.,Davis Erica E.,Katsanis Nicholas,Allori Alexander,Angrist Misha,Ashley Patricia,Bidegain Margarita,Boyd Brita,Chambers Eileen,Cope Heidi,Cotten C. Michael,Curington Theresa,Davis Erica E.,Ellestad Sarah,Fisher Kimberley,French Amanda,Gallentine William,Goldberg Ronald,Hill Kevin,Kansagra Sujay,Katsanis Nicholas,Katsanis Sara,Kurtzberg Joanne,Marcus Jeffrey,McDonald Marie,Mikati Mohammed,Miller Stephen,Murtha Amy,Perilla Yezmin,Pizoli Carolyn,Purves Todd,Ross Sherry,Sadeghpour Azita,Smith Edward,Wiener John

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference73 articles.

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