MUTATIONS MAPT 44087751 GRCh37/hg19 G A Exon 10 Point, Missense Coding Unknown; predicted benign and well-tolerated in silico. Not applicable. V300I Frontotemporal Dementia: BenignNone This rare variant was found in a genetic screen of 282 control samples from the
University of Southern CaliforniaLos Angeles, United States
Mayo Clinic JacksonvilleJacksonville, United States
West Virginia UniversityUnited States
MUTATIONS MAPT 44067400 GRCh37/hg19 rs10445337 T C Exon 6 Point, Missense Coding Unknown. Not applicable. S447P Frontotemporal Dementia: BenignNone This variant has been reported in controls and is thought to be benign (Poorkaj et al., 1998). The polymorphism resid
MUTATIONS MAPT 44067382 GRCh37/hg19 rs2258689 C T Exon 6 Point, Missense Coding Unknown. Not applicable. Y441H Frontotemporal Dementia: BenignNone This variant has been reported in healthy controls and is thought to be benign (Poorkaj et al., 1998). The polymorphis
PAPER Labbé C, Rayaprolu S, Soto-Ortolaza A, Ogaki K, Uitti RJ, Wszolek ZK, Ross OA
Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S147-9. PubMed: 24262168
PAPER Bezard E, Fernagut PO
Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S17-9. PubMed: 24262174
PAPER Alafuzoff I, Parkkinen L
Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S57-61. PubMed: 24262190
PAPER McCann H, Stevens CH, Cartwright H, Halliday GM
Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S62-7. PubMed: 24262191
PAPER Kim JN, Kim MK, Cho KS, Choi CS, Park SH, Yang SI, Joo SH, Park JH, Bahn G, Shin CY, Lee HJ, Han SH, Kwon KJ
Biomol Ther (Seoul). 2013 May 30;21(3):222-8. PubMed: 24265868