| Type II e. |
in a hypothesis test, failing to reject the null hypothesis when it is false; the probability of a Type II error is denoted by β.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type II h. |
that resulting from antibody-antigen interactions on cell surfaces; see type II hypersensitivity reaction, under hypersensitivity reaction, at reaction. Called also antibody-mediated h.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type II i. |
i.-γ.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type II t. |
DNA topoisomerase (ATP-hydrolyzing).
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type III |
amylo-1,6-glucosidase deficiency: an autosomal recessive disorder caused by a defect in the debranching enzyme in muscle, liver, or both; defects in the liver enzyme are characterized by hepatomegaly and hypoglycemia, while defects in the muscle enzyme are characterized by progressive muscle wasting and weakness. Heart and skeletal muscle are also frequently affected. Called also debrancher deficiency.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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