A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype.

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@article{5952140e2b94473bbed582471e41c599,

title = "A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype.",

author = "M. Sironi and S. Corti and F. Locatelli and R. Cagliani and Comi, {G. P.}",

year = "2001",

month = mar,

language = "English",

volume = "17",

pages = "239",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "John Wiley and Sons Inc.",

number = "3",

}

TY - JOUR

T1 - A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype.

AU - Sironi, M.

AU - Corti, S.

AU - Locatelli, F.

AU - Cagliani, R.

AU - Comi, G. P.

PY - 2001/3

Y1 - 2001/3

UR - http://www.scopus.com/inward/record.url?scp=18044400501&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=18044400501&partnerID=8YFLogxK

M3 - Article

C2 - 11241855

AN - SCOPUS:18044400501

VL - 17

SP - 239

JO - Human Mutation

JF - Human Mutation

SN - 1059-7794

IS - 3

ER -