A Japanese family with FEOM1-linked congenital fibrosis of the extraocular muscles type 1 associated with spinal canal stenosis and refinement of the FEOM1 critical region

Neuromuscular Disorders

Volumn 13, Issue 6, 2003, Pages 472-478

  Uyama, E ^a   Yamada, K ^b   Kawano, H ^a   Chan, W M ^b   Andrews, C ^b   Yoshioka, M ^c   Uchino, M ^a   Engle, E C ^b  

^a KUMAMOTO UNIV SCHOOL OF MEDICINE   (Japan)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c Kobe City Pediat/Gen Rehab C   (Japan)

Author keywords

12p11.2 q12; Congenital fibrosis of the extraocular muscles; Congenital fibrosis of the extraocular muscles type 1; Familial spinal canal stenosis; FEOM1

Indexed keywords

GENOMIC DNA;

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; DISEASE ASSOCIATION; DNA FINGERPRINTING; DNA FLANKING REGION; DNA RECOMBINATION; EXTRAOCULAR MUSCLE; FEMALE; GAZE PARALYSIS; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; MALE; MICROSATELLITE MARKER; MYOFIBROSIS; POLYMORPHIC LOCUS; PRIORITY JOURNAL; PTOSIS; VERTEBRAL CANAL STENOSIS;

EID: 0041663565     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(03)00065-8     Document Type: Article

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