Mutations in the AMPA receptor complex protein FRRS1L cause an inherited Huntington-like chorea-dementia syndrome

Journal article

Open access

Peer reviewed

M. Salih, M. Madeo, L. Fields, M. Seidahmed, H. El Khashab, M. Hamad, T. Jepperson, P. Crotwell, A. Myers, Y. Sun, …

Journal of the neurological sciences, Vol.357, pp.e286-e287

15/10/2015

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https://doi.org/10.1016/j.jns.2015.08.1000View

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Title: Mutations in the AMPA receptor complex protein FRRS1L cause an inherited Huntington-like chorea-dementia syndrome
Creators - without role: M. Salih - King Saud University
M. Madeo - Sanford Research
L. Fields - Sanford Research
M. Seidahmed - Security Forces Hospital
H. El Khashab - King Saud University
M. Hamad - King Saud University
T. Jepperson - Sanford Research
P. Crotwell - Sanford Children's Specialty Clinic
A. Myers - Sanford Children's Specialty Clinic
Y. Sun - University of Sioux Falls
B. Singh - University of Sioux Falls
M. Kruer - Sanford Research
Publication Details: Journal of the neurological sciences, Vol.357, pp.e286-e287
Publisher: Elsevier B.V
Identifiers: 9924275108331
Academic Unit: King Saud University
Language: English
Resource Type: Journal article