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                                       Details for article 45 of 52 found articles
 
 
  Syndromic Hearing Loss in Moroccan families is associated to homozygous missense variants in COL4A3 and MASP1
 
 
Title: Syndromic Hearing Loss in Moroccan families is associated to homozygous missense variants in COL4A3 and MASP1
Author: Amalou, Ghita
Aitraise, Imane
Bouzidi, Aymane
Essadssi, Soukaina
Charif, Majida
Kandil, Mostafa
Boucher, Sophie
Lenaers, Guy
Barakat, Abdelhamid
Appeared in: Human gene
Paging: Volume 33 () nr. C pages p.
Year: 2022
Contents:
Publisher: Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 45 of 52 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands