Published in
Wiley, Birth Defects Research, 7(110), p. 598-602, 2018
DOI: 10.1002/bdr2.1204
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A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern
Journal article published in 2018 by
Suzanne Chartier 
,
Caroline Alby,
Lucile Boutaud,
Sophie Thomas,
Nadia Elkhartoufi,
Jelena Martinovic,
Josseline Kaplan,
Alexandra Benachi,
Didier Lacombe ,
Pascale Sonigo,
Séverine Drunat,
Michel Vekemans,
Joël Agenor,
Férechté Encha Razavi,
Tania Attie-Bitach
,
Caroline Alby,
Lucile Boutaud,
Sophie Thomas,
Nadia Elkhartoufi,
Jelena Martinovic,
Josseline Kaplan,
Alexandra Benachi,
Didier Lacombe ,
Pascale Sonigo,
Séverine Drunat,
Michel Vekemans,
Joël Agenor,
Férechté Encha Razavi,
Tania Attie-Bitach
This paper is made freely available by the publisher.
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