CRASH syndrome: Mutations in L1CAM correlate with severity of the disease

Neuropediatrics

Volumn 28, Issue 3, 1997, Pages 175-178

  Yamasaki, M ^a,c   Thompson, P ^b   Lemmon, V ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CASE WESTERN RESERVE UNIVERSITY   (United States)

^c OSAKA NATIONAL HOSPITAL   (Japan)

Author keywords

L1CAM; MASA syndrome; X linked hydrocephalus

Indexed keywords

NERVE CELL ADHESION MOLECULE;

ARTICLE; CHILD; COMPARATIVE STUDY; CORPUS CALLOSUM; CYTOPLASM; DEATH; DISEASE SEVERITY; FEMALE; GENE MUTATION; HUMAN; HYDROCEPHALUS; HYPOPLASIA; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; MOLECULAR GENETICS; PARAPLEGIA; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DOMAIN; SPASTICITY; THUMB MALFORMATION; X CHROMOSOME LINKAGE;

EID: 0030858735     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-973696     Document Type: Article

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