Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
JN Haslett, D Sanoudou, AT Kho, M Han, RR Bennett… - Neurogenetics, 2003 - Springer
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
[PDF][PDF] Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
JN Haslett, D Sanoudou, AT Kho, M Han… - Neurogenetics, 2003 - academia.edu
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
JN Haslett, D Sanoudou, AT Kho, M Han, RR Bennett… - neurogenetics, 2002 - infona.pl
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
JN Haslett, D Sanoudou, AT Kho, M Han, RR Bennett… - Neurogenetics, 2003 - elibrary.ru
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
JN Haslett, D Sanoudou, AT Kho, M Han… - …, 2003 - search.proquest.com
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
[引用][C] Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
JN HASLETT, D SANOUDOU, AT KHO… - Neurogenetics …, 2003 - pascal-francis.inist.fr
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle CNRS Inist
Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search Advanced …
Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search Advanced …
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
JN Haslett, D Sanoudou, AT Kho, M Han… - …, 2003 - pubmed.ncbi.nlm.nih.gov
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle.
JN Haslett, D Sanoudou, AT Kho, M Han… - Neurogenetics, 2003 - europepmc.org
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
[PDF][PDF] Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
JN Haslett, D Sanoudou, AT Kho, M Han… - …, 2003 - researchgate.net
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
JN Haslett, D Sanoudou, AT Kho, M Han, RR Bennett… - neurogenetics, 2003 - infona.pl
. The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin
gene, leading to absence of the corresponding protein, disruption of the dystrophin …
gene, leading to absence of the corresponding protein, disruption of the dystrophin …