Genotype-phenotype correlation in L1 associated diseases

Journal of Medical Genetics

Volumn 35, Issue 5, 1998, Pages 399-404

  Fransen, Erik ^a   Van Camp, Guy ^a   D'Hooge, Rudi ^b   Vits, Lieve ^a   Willems, Patrick J ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

Cell adhesion molecule; Genotype phenotype correlation; L1; Mental retardation

Indexed keywords

MUTANT PROTEIN; NERVE CELL ADHESION MOLECULE;

ARTICLE; CORPUS CALLOSUM; GENE MUTATION; GENOTYPE; HUMAN; HYDROCEPHALUS; HYPOPLASIA; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; MISSENSE MUTATION; NEUROLOGIC DISEASE; PHENOTYPE; PRIORITY JOURNAL; SPASTIC PARAPLEGIA; SYNDROME; THUMB MALFORMATION;

EID: 0031898231     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.35.5.399     Document Type: Article

References (12)

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