Outline structure of the human L1 cell adhesion molecule and the sites where mutations cause neurological disorders

EMBO Journal

Volumn 15, Issue 22, 1996, Pages 6050-6059

  Bateman, Alex ^a   Jouet, Monique ^a   MacFarlane, John ^a   Du, Jian Sheng ^a   Kenwrick, Susan ^a   Chothia, Cyrus ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

Fibronectin type III; I set; Immunoglobulin superfamily; Telokin; X linked hydrocephalus

Indexed keywords

NERVE CELL ADHESION MOLECULE;

ARTICLE; CONFORMATION; HUMAN; HYDROGEN BOND; MISSENSE MUTATION; NERVOUS SYSTEM DEVELOPMENT; NEUROLOGIC DISEASE; PRIORITY JOURNAL; PROTEIN SECONDARY STRUCTURE; RESIDUE ANALYSIS; SURFACE PROPERTY; UNIVERSITY;

EID: 0029957549     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1002/j.1460-2075.1996.tb00993.x     Document Type: Article

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