Literature DB >> 709905

Autosomal dominantly inherited adductor laryngeal paralysis--a new syndrome with a suggestion of linkage to HLA.

M Mace, E Williamson, D Worgan.   

Abstract

A family is reported with autosomal dominantly inherited congenital bilateral adductor paralysis of the larynx. This disorder has apparently not been described previously. A search for linkage in this family with the loci for 19 other genetic markers showed a suggestion of linkage with HLA and GLO, and accordingly a suggestion that the locus for this disorder may be assigned to chromosome 6.

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Year:  1978        PMID： 709905     DOI： 10.1111/j.1399-0004.1978.tb02145.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  3 in total

1.  Familial congenital laryngeal abductor paralysis: different expression in a family with one male and three females affected.

Authors:  A Schinzel; E Hof; P Dangel; W Robinson
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

2.  Distal spinal and bulbar muscular atrophy caused by dynactin mutation.

Authors:  Imke Puls; Shin J Oh; Charlotte J Sumner; Karen E Wallace; Mary Kay Floeter; Eric A Mann; William R Kennedy; Gwen Wendelschafer-Crabb; Alexander Vortmeyer; Richard Powers; Kimberly Finnegan; Erika L F Holzbaur; Kenneth H Fischbeck; Christy L Ludlow
Journal:  Ann Neurol       Date:  2005-05       Impact factor: 10.422

3.  Hereditary distal spinal muscular atrophy with vocal cord paralysis.

Authors:  I D Young; P S Harper
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-05       Impact factor: 10.154
  3 in total

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