Heterozygous HMGB1 loss‐of‐function variants are associated with developmental delay and microcephaly
Journal article published in 2021 by
Kévin Uguen 
,
Séverine Audebert‐Bellanger,
Kilannin Krysiak ,
Eléonore Viora‐Dupont,
Sylvia Redon,
Caroline Benech,
Frederic Tran Mau‐Them ,
Julie Neidich,
Sophie Rondeau,
Celia Azevedo Soares,
Natáliya Tkachenko,
Ibrahim Elsharkawi,
Shivarajan M. Amudhavalli,
Kendra Engleman,
Jorge L. Granadillo
and other authors.
,
Séverine Audebert‐Bellanger,
Kilannin Krysiak ,
Eléonore Viora‐Dupont,
Sylvia Redon,
Caroline Benech,
Frederic Tran Mau‐Them ,
Julie Neidich,
Sophie Rondeau,
Celia Azevedo Soares,
Natáliya Tkachenko,
Ibrahim Elsharkawi,
Shivarajan M. Amudhavalli,
Kendra Engleman,
Jorge L. Granadillo
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 