Lysosomal dysfunction and other pathomechanisms in FTLD: evidence from progranulin genetics and biology
It has been more than a decade since heterozygous loss-of-function mutations in the
progranulin gene (GRN) were first identified as an important genetic cause of frontotemporal …
progranulin gene (GRN) were first identified as an important genetic cause of frontotemporal …
Lysosomal Dysfunction and Other Pathomechanisms in FTLD: Evidence from Progranulin Genetics and Biology
X Zhou, T Kukar, R Rademakers - Frontotemporal Dementias - Springer
Frontotemporal lobar degeneration (FTLD) is a complex disease, characterized by
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
[HTML][HTML] Lysosomal Dysfunction and Other Pathomechanisms in FTLD: Evidence from Progranulin Genetics and Biology
X Zhou, T Kukar, R Rademakers - Advances in experimental …, 2021 - ncbi.nlm.nih.gov
Frontotemporal lobar degeneration (FTLD) is a complex disease, characterized by
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
[PDF][PDF] Lysosomal Dysfunction and Other Pathomechanisms in FTLD: Evidence from Progranulin Genetics and Biology
X Zhou, T Kukar, R Rademakers - Frontotemporal Dementias - researchgate.net
Frontotemporal lobar degeneration (FTLD) is a complex disease, characterized by
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
[引用][C] Lysosomal dysfunction and other pathomechanisms in FTLD: evidence from progranulin genetics and biology
X Zhou, T Kukar, R Rademakers - … medicine and biology …, 2021 - repository.uantwerpen.be
Lysosomal dysfunction and other pathomechanisms in FTLD : evidence from progranulin
genetics and biology - Institutional Repository University of Antwerp Publication Title …
genetics and biology - Institutional Repository University of Antwerp Publication Title …
Lysosomal Dysfunction and Other Pathomechanisms in FTLD: Evidence from Progranulin Genetics and Biology
X Zhou, T Kukar, R Rademakers - Advances in …, 2021 - mayoclinic.elsevierpure.com
It has been more than a decade since heterozygous loss-of-function mutations in the
progranulin gene (GRN) were first identified as an important genetic cause of frontotemporal …
progranulin gene (GRN) were first identified as an important genetic cause of frontotemporal …
Lysosomal Dysfunction and Other Pathomechanisms in FTLD: Evidence from Progranulin Genetics and Biology.
X Zhou, T Kukar, R Rademakers - Advances in Experimental …, 2021 - europepmc.org
Frontotemporal lobar degeneration (FTLD) is a complex disease, characterized by
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
Lysosomal Dysfunction and Other Pathomechanisms in FTLD: Evidence from Progranulin Genetics and Biology
X Zhou, T Kukar, R Rademakers - … : Emerging Milestones of the …, 2021 - books.google.com
Frontotemporal lobar degeneration (FTLD) is a complex disease, characterized by
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
progressive degeneration of frontal and temporal lobes and extensive neuroinflammation …
Lysosomal Dysfunction and Other Pathomechanisms in FTLD: Evidence from Progranulin Genetics and Biology
X Zhou, T Kukar, R Rademakers - … medicine and biology, 2021 - pubmed.ncbi.nlm.nih.gov
It has been more than a decade since heterozygous loss-of-function mutations in the
progranulin gene (GRN) were first identified as an important genetic cause of frontotemporal …
progranulin gene (GRN) were first identified as an important genetic cause of frontotemporal …