reference/7919660

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publicationName	Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
startingPage	112
bibliographicCitation	Rieckmann T, Zhuang L, Flück CE, Trueb B. Characterization of the first FGFRL1 mutation identified in a craniosynostosis patient. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2009 Feb;1792(2):112–21. doi: 10.1016/j.bbadis.2008.11.006.
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date	200902
identifier	https://pubmed.ncbi.nlm.nih.gov/19056490 https://doi.org/10.1016/j.bbadis.2008.11.006
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language	English
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title	Characterization of the first FGFRL1 mutation identified in a craniosynostosis patient
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