INHERITED DELETION AT DUCHENNE DYSTROPHY LOCUS IN NORMAL MALE

The Lancet

Volumn 333, Issue 8636, 1989, Pages 496-497

  Bartlett, R J ^a   Walker, A P ^a   Laing, N G ^b   Koh, J ^c   Secore, S L ^a   Pericak Vance, M A ^a   Yamaoka, L H ^a   Kandt, R ^a   Speer, M C ^a   Hung, W Y ^a   Siddique, T ^a   Roses, A D ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b Australian Neuromuscular Research Institute   (Australia)

^c UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84919579955     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(89)91394-9     Document Type: Letter

References (6)

1. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organisation of the DMD gene in normal and affected individuals
2. A cDNA clone from the Duchenne/Becker muscular dystrophy gene
3. Duchenne muscular dystrophy: high frequency of deletions
4. Inherited deletion at Duchenne dystrophy locus in normal male
5. Transcription of the dystrophin gene in human muscle and non-muscle tissues