Published in
Wiley, The American Journal of Medical Genetics - Part A, 5(173), p. 1396-1399, 2017
DOI: 10.1002/ajmg.a.38214
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Further evidence for specific IFIH1 mutation as a cause of Singleton-Merten syndrome with phenotypic heterogeneity
Journal article published in 2017 by
Maria Pettersson 
,
Birgitta Bergendal,
Johanna Norderyd,
Daniel Nilsson ,
Britt-Marie Anderlid,
Ann Nordgren,
Anna Lindstrand
,
Birgitta Bergendal,
Johanna Norderyd,
Daniel Nilsson ,
Britt-Marie Anderlid,
Ann Nordgren,
Anna Lindstrand
This paper is made freely available by the publisher.
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