40th ENMC sponsored international workshop: Nemaline myopathy 2-4 February 1996, Naarden, The Netherlands

Neuromuscular Disorders

Volumn 6, Issue 5, 1996, Pages 389-391

  Wallgren Pettersson, Carina ^a   Laing, Nigel ^b  

^a UNIVERSITY OF HELSINKI   (Finland)

^b PATHWEST LABORATORY MEDICINE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL FEATURE; CONFERENCE PAPER; HISTOLOGY; MOLECULAR GENETICS; NEMALINE MYOPATHY; PRIORITY JOURNAL; WORKSHOP;

EID: 0030273670     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/0960-8966(96)00354-9     Document Type: Conference Paper

References (6)

1. Conen P E, Murphy E G, Donohue W L. Light and electron microscopic studies of "myogranules" in a child with hypotonia and muscle weakness. Can Med Assoc J 1963; 89: 983-986.
2. Barohn R, Jackson C E, Kagan-Hallet K S. Neonatal nemaline myopathy with abundant intranuclear rods. Neuromusc Disord 1994; 4: 513-520.
3. Laing N G, Wilton S D, Akkari P A, Dorosz S, Boundy K, Kneebone C S, Blumbergs P C, White S, Watkins H, Love D R, Haan E. A mutation in the alpha-tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1. Nature Genet 1995; 9: 75-79.
4. Shy G M, Engel W K, Somers J E, Wanko T. Nemaline myopathy. A new congenital myopathy. Brain 1963; 86: 793-810.
5. Wallgren-Pettersson C, Kääriäinen H, Rapola J, Salmi T, Jääskeläinen J, Donner M. Genetics of congenital nemaline myopathy - a study of ten families. J Med Genet 1990; 27: 480-487.
6. Wallgren-Pettersson C, Avela K, Marchand S, Kolehmainen J, Tahvanainen E, Juul Hansen F, Muntoni F, Dubowitz V, de Visser M, van Langen I M, Laing N G, Fauré S, de la Chapelle A. A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis. Neuromusc Disord 1995; 6: 441-443.