Hutchinson–Gilford progeria syndrome: a premature aging disease

MS Ahmed, S Ikram, N Bibi, A Mir - Molecular neurobiology, 2018 - Springer
Progeria is sporadic, very rare, autosomal dominant, deadly childhood disorder. It is one of
the progeroid syndromes also known as Hutchinson–Gilford progeria syndrome (HGPS) …
被引用次数：124 相关文章
[PDF] academia.edu

[PDF][PDF] Hutchinson–Gilford Progeria Syndrome: A Premature Aging

MS Ahmed, S Ikram, N Bibi, A Mir - DNA, 2017 - academia.edu
Progeria is sporadic, very rare, autosomal dominant, deadly childhood disorder. It is one of
the progeroid syndromes also known as Hutchinson–Gilford progeria syndrome (HGPS) …
[PDF] researchgate.net

[PDF][PDF] Hutchinson–Gilford Progeria Syndrome: A Premature Aging

MS Ahmed, S Ikram, N Bibi, A Mir - DNA, 2017 - researchgate.net
Progeria is sporadic, very rare, autosomal dominant, deadly childhood disorder. It is one of
the progeroid syndromes also known as Hutchinson–Gilford progeria syndrome (HGPS) …

Hutchinson-Gilford Progeria Syndrome: A Premature Aging Disease.

MS Ahmed, S Ikram, N Bibi, A Mir - Molecular Neurobiology, 2017 - europepmc.org
Progeria is sporadic, very rare, autosomal dominant, deadly childhood disorder. It is one of
the progeroid syndromes also known as Hutchinson-Gilford progeria syndrome (HGPS) …

Hutchinson-Gilford Progeria Syndrome: A Premature Aging Disease

MS Ahmed, S Ikram, N Bibi… - Molecular neurobiology, 2018 - pubmed.ncbi.nlm.nih.gov
Progeria is sporadic, very rare, autosomal dominant, deadly childhood disorder. It is one of
the progeroid syndromes also known as Hutchinson-Gilford progeria syndrome (HGPS) …

Hutchinson–Gilford Progeria Syndrome: A Premature Aging Disease

MS Ahmed, S Ikram, N Bibi, A Mir - Molecular Neurobiology, 2018 - search.proquest.com
Progeria is sporadic, very rare, autosomal dominant, deadly childhood disorder. It is one of
the progeroid syndromes also known as Hutchinson–Gilford progeria syndrome (HGPS) …