Mohney, Brian G <br/><br/>
A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.  [electronic resource] 

 -  Ophthalmology  Jun 2011 
 - 1137-44 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1549-4713 
<br/><br/><label>Standard No.: </label>10.1016/j.ophtha.2010.10.009  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Adult<br/>Aged<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 3<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>Eye Abnormalities--genetics<br/>Female<br/>Follow-Up Studies<br/>Genetic Predisposition to Disease<br/>Humans<br/>Infant<br/>Laminin--genetics<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Myasthenic Syndromes, Congenital<br/>Nephrotic Syndrome<br/>Pedigree<br/>Phenotype<br/>Pupil Disorders--genetics<br/>Retrospective Studies<br/>Young Adult