Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype

C Ruhno, VL McGovern, MR Avenarius, PJ Snyder… - Human genetics, 2019 - Springer
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …
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Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype.

C Ruhno, VL McGovern, MR Avenarius… - Human …, 2019 - europepmc.org
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …

Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype

C Ruhno, VL McGovern, MR Avenarius… - Human …, 2019 - pubmed.ncbi.nlm.nih.gov
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …

Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype

C Ruhno, VL McGovern, MR Avenarius, PJ Snyder… - Human …, 2019 - go.gale.com
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …

Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype

C Ruhno, VL McGovern, MR Avenarius… - Human …, 2019 - search.proquest.com
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …

Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype.

C Ruhno, VL McGovern, MR Avenarius… - Human …, 2019 - search.ebscohost.com
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …
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[HTML][HTML] Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype

C Ruhno, VL McGovern, MR Avenarius… - Human …, 2019 - ncbi.nlm.nih.gov
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …

Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype

C Ruhno, VL McGovern, MR Avenarius… - Human …, 2019 - ohiostate.elsevierpure.com
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …
[PDF] unimi.it

[PDF][PDF] Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype

C Ruhno, VL McGovern, MR Avenarius, PJ Snyder… - Human …, 2019 - air.unimi.it
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …

Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype.

C Ruhno, VL McGovern, MR Avenarius… - Human …, 2019 - europepmc.org
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or
mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed …