Add to ORKGSIGLEAvailable from British Library Document Supply Centre-DSC:DXN025572 / BLDSC - British Library Document Supply CentreGBUnited Kingdo
The myotonic dystrophies are a group of dominantly inherited disorders characterized by muscle wasti...
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CT...
Myotonic dystrophy (DM) is an autosomal dominant ge-netic disease caused by an unstable CTG repeat s...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN032683 / BLDSC - British Library D...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN031165 / BLDSC - British Library D...
We have analyzed the intracellular localization of transcripts from the myotonin protein kinase (Mt-...
Contains fulltext : 233612.pdf (Publisher’s version ) (Open Access)Radboud Univers...
Myotonic dystrophy is an autosomal dominant, multisystemic disease characterized by progressive musc...
Myotonic dystrophy (DM), an autosomal dominant disorder mapping to human chromosome 19q13.3, is the ...
Myotonic dystrophy (DM), an autosomal dominant disorder mapping to human chromosome 19q13.3, is the ...
Myotonic dystrophy (DM)—the most common form of muscular dystrophy in adults, affecting 1/8,000 indi...
Abstract Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are human neuromuscular disorders associat...
29 p. A THESIS Presented to the Department of Chemistry and the Clark Honors College of the Universi...
The expansion of gene-specific trinucleotide repeats is responsible for a growing list of human diso...
The expansion of gene-specific trinucleotide repeats is responsible for a growing list of human diso...
The myotonic dystrophies are a group of dominantly inherited disorders characterized by muscle wasti...
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CT...
Myotonic dystrophy (DM) is an autosomal dominant ge-netic disease caused by an unstable CTG repeat s...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN032683 / BLDSC - British Library D...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN031165 / BLDSC - British Library D...
We have analyzed the intracellular localization of transcripts from the myotonin protein kinase (Mt-...
Contains fulltext : 233612.pdf (Publisher’s version ) (Open Access)Radboud Univers...
Myotonic dystrophy is an autosomal dominant, multisystemic disease characterized by progressive musc...
Myotonic dystrophy (DM), an autosomal dominant disorder mapping to human chromosome 19q13.3, is the ...
Myotonic dystrophy (DM), an autosomal dominant disorder mapping to human chromosome 19q13.3, is the ...
Myotonic dystrophy (DM)—the most common form of muscular dystrophy in adults, affecting 1/8,000 indi...
Abstract Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are human neuromuscular disorders associat...
29 p. A THESIS Presented to the Department of Chemistry and the Clark Honors College of the Universi...
The expansion of gene-specific trinucleotide repeats is responsible for a growing list of human diso...
The expansion of gene-specific trinucleotide repeats is responsible for a growing list of human diso...
The myotonic dystrophies are a group of dominantly inherited disorders characterized by muscle wasti...
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CT...
Myotonic dystrophy (DM) is an autosomal dominant ge-netic disease caused by an unstable CTG repeat s...