Work

CMT4A: Identification of a Hispanic GDAP1 founder mutation

Year: 2003

Type: article

Source: Annals of Neurology

DOI: 10.1002/ana.10505

Authors: Cornelius F. Boerkoel, Hiroshi Takashima, Masanori Nakagawa, Shuji Izumo, Dawna Armstrong, Ian Butler, Pedro Mancias, Sozos C. H. Papasozomenos, Lawrence Z. Stern, James R. Lupski

Institutions: Baylor College of Medicine, Kagoshima University, The University of Texas Health Science Center at Houston, University of Arizona

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Neurological Disorders and Stroke

Awards: G2875609050, G541618229, A MURINE MODEL OF SMITH-MAGENIS SYNDROME, CMT Peripheral Neuropathy: IV. Genes and Pathogenesis

OpenAlex ID: W2108760445

FWCI: 2.315

Cites: 22

Cited by: 67

Related to: 10