LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis

被引：0

作者：

Kirsten M. Farncombe

Emily Thain

Carolina Barnett-Tapia

Hamid Sadeghian

Raymond H. Kim

机构：

[1] University Health Network,Toronto General Hospital Research Institute

[2] University Health Network,Bhalwani Familial Cancer Clinic, Princess Margaret Cancer Centre

[3] University Health Network,Division of Neurology, Department of Medicine

[4] University of Toronto,Ellen and Martin Prossermann Centre for Neuromuscular Diseases

[5] Toronto General Hospital,Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre

[6] University Health Network,Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Ontario Institute for Cancer Research, Department of Medicine

[7] University Health Network,undefined

[8] Sinai Health System,undefined

[9] University of Toronto,undefined

来源：

BMC Medical Genomics | / 15卷

关键词：

Noonan syndrome; Neurofibromas; Whole exome sequencing;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

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