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Specific killing of Rb mutant cancer cells by inactivating TSC2.
NKG2D receptors induced by IL-15 costimulate CD28-negative effector CTL in the tissue microenvironment.
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci.
Who keeps the gate?
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.
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Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers. Neurogenetics. 1998 Dec; 2(1):55-60.
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PubMed
subject areas
Age of Onset
Chromosome Mapping
Chromosomes, Human, Pair 15
Disease Progression
Female
Genes, Recessive
Genetic Linkage
Genetic Markers
Humans
Male
Microsatellite Repeats
Motor Neuron Disease
Pedigree
authors with profiles
Afif Hentati