{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,1]],"date-time":"2025-10-01T16:19:17Z","timestamp":1759335557773},"reference-count":39,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2005,6,3]],"date-time":"2005-06-03T00:00:00Z","timestamp":1117756800000},"content-version":"vor","delay-in-days":4536,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Genetic Epidemiology"],"published-print":{"date-parts":[[1993,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We have previously reported a large Israili\u2010Arab pedigree with sensorineural deafness possibly determined simultaneously by two loci\u2010one mitochondrial, and one autosomal recessive. This was analyzed by extending classic segregation analysis methods to the many nuclear families derived from the maternal line pedigree. Here we expand this pedigree and extend our analysis by using the regressive models for segregation analysis on the entire pedigree. The corresponding REGD computer program was utilized and the marrying\u2010in males' and paternal line members' affection statuses were assigned as unknown to accommodate the exclusive maternal transmission pattern. For the autosomal locus, a simple autosomal recessive (<jats:italic>q<\/jats:italic> = 0.52) model with a nearly complete penetrance (0.93) was found to be the regressive models to test the hypothesis of mitochondrial mutation occurred in a heteroplasmic distribution in the family members, this could not explain the familial aggregation in this pedigree, and an autosomal recessive locus is still required. These results provide further support for the concept that the sensorineural deafness occurring in this large Israeli\u2010Arab pedigree results from simultaneous involvement of two genes at two different loci, one mitochondrial and likely homoplasmic, and the other autosomal and recessive. \u00a9 1993 Wiley\u2010Liss. Inc.<\/jats:p>","DOI":"10.1002\/gepi.1370100102","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T02:13:57Z","timestamp":1118542437000},"page":"3-15","source":"Crossref","is-referenced-by-count":16,"title":["A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: Evidence from pedigree segregation analysis"],"prefix":"10.1002","volume":"10","author":[{"given":"Xiangdong","family":"Bu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mordechai","family":"Shohat","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lutfi","family":"Jaber","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jerome I.","family":"Rotter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,6,3]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1109\/TAC.1974.1100705"},{"key":"e_1_2_1_3_1","first-page":"733","volume-title":"Principles and Practice of Medical Genetics","author":"Beighton P","year":"1990"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1126\/science.6353578"},{"key":"e_1_2_1_5_1","doi-asserted-by":"crossref","first-page":"513","DOI":"10.1093\/genetics\/103.3.513","article-title":"An approach to population and evolutionary genetic theory for genes in mitochondria and chloroplasts, and some results","volume":"103","author":"Birkey CW","year":"1983","journal-title":"Genetics"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1093\/genetics\/121.3.613"},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/0006-291X(90)90490-E"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320180420"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.2307\/2531211"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.88.18.8198"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1002\/gepi.1370090105"},{"key":"e_1_2_1_12_1","doi-asserted-by":"publisher","DOI":"10.2307\/1426718"},{"key":"e_1_2_1_13_1","first-page":"773","article-title":"Regressive logistic models for familial diseases: A formulation assuming an underlying liability model","volume":"49","author":"Demenais FM","year":"1991","journal-title":"Am J Hum Genet"},{"key":"e_1_2_1_14_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00260866"},{"key":"e_1_2_1_15_1","first-page":"129","article-title":"Segregation analysis for complex modes of inheritance","volume":"22","author":"Elandt\u2010Johnson RC","year":"1970","journal-title":"Am J Hum Genet"},{"key":"e_1_2_1_16_1","first-page":"17","article-title":"Complex segregation analysis. 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