DOI: 10.1093/hmg/5.11.1727. An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene

An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene

10.1093/hmg/5.11.1727

Crossref journal-article

Oxford University Press (OUP)

Human Molecular Genetics (286)

Bibliography

Parsons, D. (1996). An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene. Human Molecular Genetics, 5(11), 1727â1732.

Authors 1

D. Parsons (first)

References 0 Referenced 96

None

Dates

Type	When
Created	23 years, 1 month ago (July 26, 2002, 6:20 p.m.)
Deposited	8 years ago (Aug. 23, 2017, 4:50 a.m.)
Indexed	5 months, 1 week ago (March 19, 2025, 8:13 a.m.)
Issued	28 years, 9 months ago (Nov. 1, 1996)
Published	28 years, 9 months ago (Nov. 1, 1996)
Published Print	28 years, 9 months ago (Nov. 1, 1996)

Funders 0

None

BibTeX

@article{Parsons_1996, title={An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene}, volume={5}, ISSN={1460-2083}, url={http://dx.doi.org/10.1093/hmg/5.11.1727}, DOI={10.1093/hmg/5.11.1727}, number={11}, journal={Human Molecular Genetics}, publisher={Oxford University Press (OUP)}, author={Parsons, D.}, year={1996}, month=nov, pages={1727–1732} }

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