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

Bateman, A; Jouet, M; MacFarlane, J; Du, J S; Kenwrick, S; Chothia, C

Bateman, A; Jouet, M; MacFarlane, J; Du, J S; Kenwrick, S; Chothia, C.

Affiliation

Bateman A; MRC Laboratory of Molecular Biology, Cambridge, UK.

EMBO J ; 15(22): 6050-9, 1996 Nov 15.

Article in En | MEDLINE | ID: mdl-8947027

Subject(s)

Mutation/genetics; Neural Cell Adhesion Molecules/chemistry; Neural Cell Adhesion Molecules/genetics; Amino Acid Sequence; Cell Adhesion Molecules, Neuronal/chemistry; Cell Adhesion Molecules, Neuronal/genetics; Drosophila Proteins; Fibronectins/chemistry; Fibronectins/genetics; Humans; Hydrocephalus/genetics; Leukocyte L1 Antigen Complex; Models, Molecular; Molecular Sequence Data; Muscle Proteins/chemistry; Muscle Proteins/genetics; Myosin-Light-Chain Kinase; Peptide Fragments; Peptides; Protein Conformation; Protein Folding; Protein Structure, Secondary; Sequence Alignment; X Chromosome/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neural Cell Adhesion Molecules / Mutation Type of study: Prognostic_studies Limits: Humans Language: En Journal: EMBO J Year: 1996 Document type: Article Affiliation country: United kingdom Country of publication: United kingdom

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