PLXNA1 developmental encephalopathy with syndromic features: A case report and review of the literature-Reference-Cited by-同舟云学术

PLXNA1 developmental encephalopathy with syndromic features: A case report and review of the literature

Author:

Park Kaylee¹,Seltzer Laurie E.²³,Tuttle Emily⁴,Mirzaa Ghayda M.¹⁵,Paciorkowski Alex R.²⁴⁶^ORCID

Affiliation:

1. Center for Integrative Brain Research; Seattle Children's Research Institute; Seattle Washington

2. Department of Neurology; University of Rochester Medical Center; Rochester New York

3. Strong Epilepsy Center; University of Rochester Medical Center; Rochester New York

4. Center for Neural Development and Disease; University of Rochester Medical Center; Rochester New York

5. Division of Genetic Medicine; Department of Pediatrics; University of Washington; Seattle Washington

6. Departmentsof Pediatrics, Neuroscience, and Biomedical Genetics; University of Rochester Medical Center; Rochester New York

Funder

Foundation for the National Institutes of Health

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference16 articles.

5. Dubowitz syndrome and acute lymphatic leukemia;Gröbe;Monatsschrift Kinderheilkd. Organ Dtsch Ges Für Kinderheilkd,1983

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献