Citations 2
Clinical Deep Phenotyping of ABCA7 Mutation Carriers
Campbell, Alana S., Ho, Charlotte C.G. , Atık, Merve, Allen, Mariet, Lincoln, Sarah, Malphrus, Kimberly, Nguyen, Thuy, Oatman, Stephanie R., Corda, Morgane, Conway, Olivia, Strickland, Samantha, Petersen, Ronald C., Graff-Radford, Neill R., Ertekin-Taner, Nilüfer, Dickson, Dennis W , Campbell, Alana S., Ho, Charlotte C.G. , Atık, Merve, Allen, Mariet, Lincoln, Sarah, Malphrus, Kimberly, Nguyen, Thuy, Oatman, Stephanie R., Corda, Morgane, Conway, Olivia, Strickland, Samantha, Petersen, Ronald C., Graff-Radford, Neill R., Ertekin-Taner, Nilüfer
Neurology Genetics | January 13, 2022 | Volume: 8 | Issue: 2 | Pages: No page available
ABCA7 loss-of-function variants, expression, and neurologic disease risk
Allen, Mariet , Lincoln, Sarah, Corda, M, Carrasquillo, Minerva M. , Reddy, Joseph S. , Burgess, Jeremy D. , Nguyen, Thuy , Malphrus, Kimberly G., Petersen, Ronald C. , Graff‐Radford, Neill R. , Ertekin‐Taner, Nilüfer , Lincoln, Sarah J, Corda, Morgane, Watzlawik, Jens O. , Carrasquillo, Minerva M. , Dickson, Dennis W.
Neurology Genetics | January 6, 2017 | Volume: 3 | Issue: 1 | Pages: No page available