Zobrazeno 1 - 2
of 2
pro vyhledávání: '"N. M. Marlatt"'
Publikováno v:
BMC Psychiatry, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Frontal variant frontotemporal dementia is a common cause of presenile dementia. A hexanucleotide expansion on chromosome 9 has recently been recognized as the most common genetic mutation cause of this illness. This sub-type tend
Externí odkaz:
https://doaj.org/article/0b6339b6484944d4839e8d03ddd797da
Autor:
Lena Palaniyappan, Amer M. Burhan, M. Blair, N. M. Marlatt, Udunna C. Anazodo, Elizabeth Finger
Publikováno v:
Brain and Mind Institute Researchers' Publications
BMC Psychiatry, Vol 21, Iss 1, Pp 1-6 (2021)
BMC Psychiatry
BMC Psychiatry, Vol 21, Iss 1, Pp 1-6 (2021)
BMC Psychiatry
Background Frontal variant frontotemporal dementia is a common cause of presenile dementia. A hexanucleotide expansion on chromosome 9 has recently been recognized as the most common genetic mutation cause of this illness. This sub-type tends to pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b1a2f5e2f40064013c04e939c4c7e94
https://doi.org/10.1186/s12888-021-03341-9
https://doi.org/10.1186/s12888-021-03341-9