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MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY

Known as: CMS9 
National Institutes of Health

Related topics

Related topics

5 relations
Autosomal recessive inheritanceBlepharoptosisFacial ParesisNeonatal Hypotonia

Papers overview

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1996
1996
Irrelevance of the mutated p53 gene product to tumor rejection antigen in 3-methylcholanthrene-induced fibrosarcomas.
The relevance of mutated p53 to in vivo rejection of MC-induced fibrosarcomas and/or in vitro CTL activity against these tumors… 
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