[PDF] neurology-asia.org

[PDF][PDF] Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.

M Ghanei, SH Sadat Fatemi, M Soudyab… - Neurology …, 2022 - neurology-asia.org
Spinal muscular atrophy (SMA)(OMIM#: 253300) is an autosomal recessive disorder,
resulting in symmetrical progressive weakness of skeletal and respiratory muscles and …
被引用次数：1 相关文章

Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy

M Ghanei, SHS Fatemi, M Soudyab - Neurology Asia, 2022 - neurologyasia.org
Spinal muscular atrophy (SMA)(OMIM#: 253300) is an autosomal recessive disorder,
resulting in symmetrical progressive weakness of skeletal and respiratory muscles and …

Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.

M Ghanei, SH Sadat Fatemi, M Soudyab… - Neurology …, 2022 - search.ebscohost.com
Spinal muscular atrophy (SMA)(OMIM#: 253300) is an autosomal recessive disorder,
resulting in symmetrical progressive weakness of skeletal and respiratory muscles and …
[PDF] neurologyasia.org

[PDF][PDF] Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy

J Esfehani - Neurology Asia, 2022 - neurologyasia.org
Spinal muscular atrophy (SMA)(OMIM#: 253300) is an autosomal recessive disorder,
resulting in symmetrical progressive weakness of skeletal and respiratory muscles and …
[PDF] researchgate.net

[PDF][PDF] Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy

J Esfehani - Neurology Asia, 2022 - researchgate.net
Spinal muscular atrophy (SMA)(OMIM#: 253300) is an autosomal recessive disorder,
resulting in symmetrical progressive weakness of skeletal and respiratory muscles and …

Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy

M Ghanei, SHS Fatemi, M Soudyab - Neurology Asia, 2022 - neurology-asia.org
Spinal muscular atrophy (SMA)(OMIM#: 253300) is an autosomal recessive disorder,
resulting in symmetrical progressive weakness of skeletal and respiratory muscles and …
[PDF] neurology-asia.org

[PDF][PDF] Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy

J Esfehani - Neurology Asia, 2022 - neurology-asia.org
Spinal muscular atrophy (SMA)(OMIM#: 253300) is an autosomal recessive disorder,
resulting in symmetrical progressive weakness of skeletal and respiratory muscles and …
[PDF] researchgate.net

[PDF][PDF] Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy

J Esfehani - Neurology Asia, 2022 - researchgate.net
Spinal muscular atrophy (SMA)(OMIM#: 253300) is an autosomal recessive disorder,
resulting in symmetrical progressive weakness of skeletal and respiratory muscles and …

Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy

M Ghanei, SHS Fatemi, M Soudyab - Neurology Asia, 2022 - neurologyasia.org
Spinal muscular atrophy (SMA)(OMIM#: 253300) is an autosomal recessive disorder,
resulting in symmetrical progressive weakness of skeletal and respiratory muscles and …