Patient-specific mutation of Dync1h1 in mice causes brain and behavioral deficits

Author:

Ramos Raddy L.,De Heredia Maider Michelena Beltran,Zhang Yongwei,Stout Randy F.,Tindi Jaafar O.,Wu Liching,Schwartz Gary J.,Botbol Yair M.,Sidoli Simone,Poojari Ankita,Rakowski-Anderson Tammy,Shafit-Zagardo Bridget

Funder

NCI

NIH

NSF

Publisher

Elsevier BV

Reference76 articles.

1. DYNC1H1-related disorders: a description of four new unrelated patients and a comprehensive review of previously reported variants;Amabile;Am. J. Med. Genet. A,2020

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3. Subunit composition of the human cytoplasmic dynein-2 complex;Asante;J. Cell Sci.,2014

4. Cytoplasmic dynein could be key to understanding neurodegeneration;Banks;Genome Biol.,2008

5. The clinical-phenotype continuum in DYNC1H1-related disorders-genomic profiling and proposal for a novel classification;Becker;J. Hum. Genet.,2020

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