Donner, Kati <br/><br/>
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Feb 2002 
 - 151-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0960-8966 
<br/><br/><label>Standard No.: </label>10.1016/s0960-8966(01)00252-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Biopsy<br/>DNA Primers<br/>Female<br/>Genetic Linkage<br/>Genetic Markers<br/>Haplotypes--genetics<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Muscle, Skeletal--pathology<br/>Mutation<br/>Mutation, Missense<br/>Myopathies, Nemaline--genetics<br/>Pedigree<br/>Polymorphism, Single-Stranded Conformational<br/>Protein Conformation<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Sequence Alignment<br/>Sequence Homology, Amino Acid<br/>Tropomyosin--chemistry