Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes

Neurology

Volumn 58, Issue 2, 2002, Pages 231-236

  Merlini, L ^a   Gooding, R ^b   Lochmuller H ^d,e   Muller Felber W ^e   Walter, M c ^e   Angelicheva, D ^b   Talim, B ^a   Hallmayer, J ^f   Kalaydjieva, L ^b,c  

^a RIZZOLI ORTHOPAEDIC INSTITUTE   (Italy)

^b EDITH COWAN UNIVERSITY   (Australia)

^c UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^d UNIVERSITY OF MUNICH   (Germany)

^e LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^f STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOGLOBIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CONGENITAL CATARACT; CONGENITAL CATARACT FACIAL DYSMORPHISM NEUROPATHY SYNDROME; CONTROLLED STUDY; DEMYELINATING NEUROPATHY; FACE DYSMORPHIA; FAMILY STUDY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC POLYMORPHISM; GIPSY; HAPLOTYPE; HUMAN; MALE; MARINESCO SJOGREN SYNDROME; MYOGLOBINURIA; PRIORITY JOURNAL; SYNDROME;

EID: 0037154185     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.58.2.231     Document Type: Article

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