SURGICAL TREATMENT AND EMBRYOLOGICAL CONSIDERATIONS FOR CONGENITAL MALFORMATION OF AUDITORY CONDUCTIVE APPARATUS.
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Biomedical subjects
Publications and source records attributed to S TAKAHARA.
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The heterozygous carrier state of a rare hereditary disease, acatalasemia, has been defined biochemically. Affected homozygotes have no blood catalase activity, whereas heterozygotes show activities intermediate between this inactivity and the activity of normal controls, without overlap. Pedigrees show a high frequency of consanguineous marriages.
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