Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease

Neurology

Volumn 56, Issue 8, 2001, Pages 1059-1069

  Cormand, B ^a,b,i   Pihko, H ^a   Bayes M ^a,i   Valanne, L ^a   Santavuori, P ^a   Talim, B ^c   Gershoni Baruch, R ^d   Ahmad, A ^e   Van Bokhoven, H ^g   Brunner, H G ^g   Voit, T ^h   Topaloglu, H ^c   Dobyns, W B ^f   Lehesjoki, A E ^a,b  

^a UNIVERSITY OF HELSINKI   (Finland)

^b FOLKHÄLSAN INSTITUTE OF GENETICS   (Finland)

^c HACETTEPE UNIVERSITY   (Turkey)

^d RAMBAM MEDICAL CENTER   (Israel)

^e DUKE UNIVERSITY MEDICAL CENTER   (United States)

^f UNIVERSITY OF CHICAGO   (United States)

^g RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^h UNIVERSITY OF DUISBURG ESSEN   (Germany)

ⁱ UNIVERSITAT POMPEU FABRA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ALLELISM; ARTICLE; BRAIN DISEASE; BRAIN MALFORMATION; CHILD; CHROMOSOME 1P; EYE DISEASE; GENE LOCATION; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; HAPLOTYPE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MUSCULAR DYSTROPHY; PHENOTYPE; PRIORITY JOURNAL; WALKER WARBURG SYNDROME;

EID: 0035942359     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.56.8.1059     Document Type: Article

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