Concepedia

Publication | Closed Access

The missing “link”: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation

DOI

77

Citations

35

References

2013

Year

Julia Schreml, Burak Durmaz, Özgür Çoğulu, Katharina Keupp, Filippo Beleggia, Esther Pohl, Esther Milz, Mahmut Çöker, Sema Kalkan Uçar, Gudrun Nürnberg,
Human Genetics

References

YearCitations

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