Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in …

E Hahnen, R Forkert, C Marke… - Human molecular …, 1995 - academic.oup.com
Proximal spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular
disorder characterized by degeneration of anterior horn cells in the spinal cord leading to …
被引用次数：349 相关文章

Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in …

E Hahnen, R Forkert, C Marke… - Human Molecular …, 1995 - europepmc.org
Proximal spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular
disorder characterized by degeneration of anterior horn cells in the spinal cord leading to …

Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in …

E Hahnen, R Forkert, C Marke… - Human Molecular …, 1995 - elibrary.ru
Proximal spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular
disorder characterized by degeneration of anterior horn cells in the spinal cord leading to …

Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in …

E Hahnen, R Forkert, C Marke… - Human molecular …, 1995 - pubmed.ncbi.nlm.nih.gov
Proximal spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular
disorder characterized by degeneration of anterior horn cells in the spinal cord leading to …

[引用][C] Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN …

E Hahnen, R Forkert, C Marke… - Human Molecular …, 1995 - cir.nii.ac.jp
Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal
muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected …

[引用][C] Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN …

E HAHNEN, R FORKERT, C MARKE… - Human molecular …, 1995 - pascal-francis.inist.fr
Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal
muscular atrophy : evidence of homozygous deletions of the SMN gene in unaffected …
[PDF] researchgate.net

[PDF][PDF] Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN …

E Hahnen, R Forkert, C Marke… - Human Molecular …, 1995 - researchgate.net
Proximal spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular
disorder characterized by degeneration of anterior horn cells In the spinal cord leading to …

[引用][C] Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN …

E HAHNEN, R FORKERT, C MARKE… - Human molecular …, 1995 - Oxford University Press