Structural insight into C9orf72 hexanucleotide repeat expansions: Towards new therapeutic targets in FTD-ALS

V Kumar, A Islam, F Ahmad, MI Hassan - Neurochemistry International, 2016 - Elsevier
Hexanucleotide repeat expansions,(G4C2) in the C9orf72 gene are considered as the
single most common genetic cause of both frontotemporal dementia (FTD) and amyotrophic …
被引用次数：27 相关文章

Structural insight into C9orf72 hexanucleotide repeat expansions: Towards new therapeutic targets in FTD-ALS.

V Kumar, T Kashav, A Islam, F Ahmad… - Neurochemistry …, 2016 - europepmc.org
Hexanucleotide repeat expansions,(G4C2) in the C9orf72 gene are considered as the
single most common genetic cause of both frontotemporal dementia (FTD) and amyotrophic …

Structural insight into C9orf72 hexanucleotide repeat expansions: Towards new therapeutic targets in FTD-ALS

V Kumar, T Kashav, A Islam… - Neurochemistry …, 2016 - pubmed.ncbi.nlm.nih.gov
Hexanucleotide repeat expansions,(G4C2) in the C9orf72 gene are considered as the
single most common genetic cause of both frontotemporal dementia (FTD) and amyotrophic …

[引用][C] Structural insight into C9orf72 hexanucleotide repeat expansions: Towards new therapeutic targets in FTD-ALS

V Kumar - Neurochemistry International, 2016 - cir.nii.ac.jp
Structural insight into C9orf72 hexanucleotide repeat expansions: Towards new therapeutic
targets in FTD-ALS | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細 …

Structural insight into C9orf72 hexanucleotide repeat expansions: Towards new therapeutic targets in FTD-ALS

V Kumar, A Islam, F Ahmad, MI Hassan - Neurochemistry International, 2016 - infona.pl
Hexanucleotide repeat expansions,(G4C2) in the C9orf72 gene are considered as the
single most common genetic cause of both frontotemporal dementia (FTD) and amyotrophic …