Meins, M <br/><br/>
Heterozygous 'null allele' mutation in the human peripherin/RDS gene.  [electronic resource] 

 -  Human molecular genetics  Dec 1993 
 - 2181-2 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/2.12.2181  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Animals<br/>Arginine<br/>Base Sequence<br/>Exons<br/>Genetic Carrier Screening<br/>Humans<br/>Intermediate Filament Proteins--genetics<br/>Male<br/>Membrane Glycoproteins<br/>Mice<br/>Middle Aged<br/>Mutation<br/>Nerve Tissue Proteins<br/>Neuropeptides--genetics<br/>Peripherins<br/>Polymerase Chain Reaction<br/>Retinal Degeneration--genetics