Carrier detection of duchenne and becker muscular dystrophy using muscle dystrophin immunohistochemistry

scientific article published on 01 December 1992

Carrier detection of duchenne and becker muscular dystrophy using muscle dystrophin immunohistochemistry is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1590/S0004-282X1992000400010
P953full work available at URLhttps://www.scielo.br/j/anp/a/rRbGRmBLy3565Nhc35dCSDr/?format=pdf&lang=en
http://www.scielo.br/pdf/anp/v50n4/10.pdf
P698PubMed publication ID1309152

P2093author name stringB. Schmidt
A. S. Oliveira
E. Bonilla
J. G. Lima
C. Minetti
A. A. Gabbai
B. H. Kiyomoto
P2860cites workSex chromatin and gene action in the mammalian X-chromosomeQ34263110
Very mild muscular dystrophy associated with the deletion of 46% of dystrophinQ34371637
Molecular biology of Duchenne and Becker's muscular dystrophy: clinical applicationsQ38686654
Dystrophin in the differentiation between Duchenne and Becker muscular dystrophies: an immunohistochemical study compared with clinical stage, serum enzymes and muscle biopsyQ41874136
P433issue4
P407language of work or nameEnglishQ1860
P921main subjectneurologyQ83042
immunohistochemistryQ899285
Becker muscular dystrophyQ2484592
P304page(s)478-485
P577publication date1992-12-01
P1433published inArquivos de Neuro-PsiquiatriaQ15750263
P1476titleCarrier detection of Duchenne and Becker muscular dystrophy using muscle dystrophin immunohistochemistry
Carrier detection of duchenne and becker muscular dystrophy using muscle dystrophin immunohistochemistry
P478volume50

Reverse relations

cites work (P2860)
Q35889152Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.
Q33679539The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol