Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome.

dc.contributor.author	THIEL, S
dc.contributor.author	Altunoglu, UMUT
dc.contributor.author	KAYSERILI, H
dc.contributor.author	TEKIN, M
dc.contributor.author	KOPARIR, Asuman
dc.contributor.author	ATIK, T
dc.contributor.author	BADEMCI, G
dc.contributor.author	FOSTER, J 2ND
dc.contributor.author	MUTLU, GY
dc.contributor.author	BOWDIN, S
dc.contributor.author	ELCIOGLU, N
dc.contributor.author	TAYFUN, GA
dc.contributor.author	ATIK, SS
dc.contributor.author	OZEN, M
dc.contributor.author	OZKINAY, F
dc.contributor.author	ALANAY, Y
dc.date.accessioned	2021-03-03T18:34:18Z
dc.date.available	2021-03-03T18:34:18Z
dc.identifier.citation	ATIK T., KOPARIR A., BADEMCI G., FOSTER J. 2. , Altunoglu U., MUTLU G., BOWDIN S., ELCIOGLU N., TAYFUN G., ATIK S., et al., "Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome.", Orphanet journal of rare diseases, cilt.10, ss.128, 2015
dc.identifier.issn	1750-1172
dc.identifier.other	vv_1032021
dc.identifier.other	av_4fcabc22-b271-4dad-99b1-a44c362daccd
dc.identifier.uri	http://hdl.handle.net/20.500.12627/56864
dc.identifier.uri	https://doi.org/10.1186/s13023-015-0345-3
dc.language.iso	eng
dc.title	Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome.
dc.type	Makale
dc.relation.journal	Orphanet journal of rare diseases
dc.contributor.department	Ege Üniversitesi , ,
dc.identifier.volume	10
dc.identifier.startpage	128
dc.identifier.endpage	128
dc.contributor.firstauthorID	182162

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