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Autosomal dominantly inherited adductor laryngeal paralysis ‐ a new syndrome with a suggestion of linkage to HLA
Author(s) -
Mace Margaret,
Williamson Elspeth,
Worgan D.
Publication year - 1978
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1978.tb02145.x
Subject(s) - genetics , locus (genetics) , genetic linkage , biology , paralysis , human leukocyte antigen , medicine , gene , surgery , antigen
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.