Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause Laing early-onset distal myopathy (MPD1)

American Journal of Human Genetics

Volumn 75, Issue 4, 2004, Pages 703-708

  Meredith, Christopher ^a   Herrmann, Ralf ^c   Parry, Cheryl ^a   Liyanage, Khema ^d,e   Dye, Danielle E ^d,e   Durling, Hayley J ^d   Duff, Rachael M ^d   Beckman, Kaye ^d,e   De Visser, Marianne ^f   Van Der Graaff, Maaike M ^f   Hedera, Peter ^g,j   Fink, John K ^g,i   Petty, Elizabeth M ^h   Lamont, Phillipa ^b   Fabian, Vicki ^b   Bridges, Leslie ^b   Voit, Thomas ^c   Mastaglia, Frank L ^d   Laing, Nigel G ^d,e  

^a EDITH COWAN UNIVERSITY   (Australia)

^b ROYAL PERTH HOSPITAL   (Australia)

^c UNIVERSITY HOSPITAL ESSEN   (Germany)

^d UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^e UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^f UNIVERSITY OF AMSTERDAM   (Netherlands)

^g UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^h UNIVERSITY OF MICHIGAN   (United States)

ⁱ VA ANN ARBOR HEALTHCARE SYSTEM   (United States)

^j VANDERBILT UNIVERSITY   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; LEUCINE; LYSINE; MYOSIN HEAVY CHAIN; PROLINE;

3' UNTRANSLATED REGION; ARTICLE; DISTAL MYOPATHY; EXON; GENE IDENTIFICATION; GENE MUTATION; HETEROZYGOSITY; PREDICTION; PRIORITY JOURNAL; SKELETAL MUSCLE;

EID: 4544374719     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/424760     Document Type: Article

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