Meyer, Jobst <br/><br/>
Mutational analysis of the connexin 36 gene (CX36) and exclusion of the coding sequence as a candidate region for catatonic schizophrenia in a large pedigree.  [electronic resource] 

 -  Schizophrenia research  Nov 2002 
 - 87-91 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0920-9964 
<br/><br/><label>Standard No.: </label>10.1016/s0920-9964(02)00206-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 15<br/>Connexins--genetics<br/>DNA Mutational Analysis<br/>Exons--genetics<br/>Gene Frequency<br/>Genetic Linkage<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Introns--genetics<br/>Mutation<br/>Open Reading Frames--genetics<br/>Pedigree<br/>Polymorphism, Genetic<br/>Regulatory Sequences, Nucleic Acid--genetics<br/>Schizophrenia, Catatonic--genetics<br/>Gap Junction delta-2 Protein