Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy

Y Sun, M Grimmler, V Schwarzer, F Schoenen… - Human …, 2005 - Wiley Online Library
The autosomal recessive spinal muscular atrophy (SMA), a neuromuscular disease and
frequent cause of early death in childhood, is caused in 96% of patients by homozygous …
被引用次数：156 相关文章

Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy

Y Sun, M Grimmler, V Schwarzer… - Human …, 2005 - pubmed.ncbi.nlm.nih.gov
The autosomal recessive spinal muscular atrophy (SMA), a neuromuscular disease and
frequent cause of early death in childhood, is caused in 96% of patients by homozygous …

Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.

Y Sun, M Grimmler, V Schwarzer, F Schoenen… - Human …, 2005 - europepmc.org
The autosomal recessive spinal muscular atrophy (SMA), a neuromuscular disease and
frequent cause of early death in childhood, is caused in 96% of patients by homozygous …

[引用][C] Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy

Y Sun, M Grimmler, V Schwarzer, F Schoenen… - Human Mutation, 2005 - cir.nii.ac.jp

Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy

Y Sun, M Grimmler, V Schwarzer, F Schoenen… - Human …, 2005 - search.proquest.com
The autosomal recessive spinal muscular atrophy (SMA), a neuromuscular disease and
frequent cause of early death in childhood, is caused in 96% of patients by homozygous …

[引用][C] Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy

Y SUN - Hum. Mutat., 2005 - cir.nii.ac.jp
Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal
muscular atrophy | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ …

[引用][C] Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy

Y SUN, M GRIMMLER, V SCHWARZER… - Human mutation, 2005 - Wiley-Liss