Literature DB >> 5970744

Marriages between the deaf and hereditary deafness in Finland.

J S Lumio, H Piirainen, P Paljakka.   

Abstract

Mesh：

Year:  1966        PMID： 5970744     DOI： 10.3109/00016486609119572

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN： 0001-6489            Impact factor:   1.494


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  1 in total

1.  Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes.

Authors:  K Sigvard Olsson; Olof Wålinder; Ulf Jansson; Maria Wilbe; Marie-Louise Bondeson; Eva-Lena Stattin; Ruma Raha-Chowdhury; Roger Williams
Journal:  Hereditas       Date:  2017-12-19       Impact factor: 3.271
  1 in total

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