Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene

Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene Publisher Pubmed

Youssefian L^{1, 2} ; Vahidnezhad H^{1, 3} ; Aghighi Y⁴ ; Ziaee V^{4, 5} ; Zeinali S^{3, 6} ; Abiri M^{2, 3} ; Uitto J¹

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1. Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, 233 S. 10th Street, Suite 450 BLSB, Philadelphia, 19107, PA, United States
2. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
3. Biotechnology Research Center, Department of Molecular Medicine, Pasteur Institute of Iran, Tehran, Iran
4. Department of Pediatrics, Imam Khomeini Hospital, Tehran University of Medial Sciences, Tehran, Iran
5. Rheumatology Research Center, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
6. Kawsar Human Genetics Research Center, Tehran, Iran

Source: Acta Dermato-Venereologica Published:2017

Abstract

[No abstract available]

2. Infantile Systemic Hyalinosis in an Iranian Family With a Mutation in the Cmg2/Antxr2 Gene, Clinical and Experimental Dermatology (2015)

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Vahid Ziaee (2)

Style	Citing Format
MLA	Youssefian L, et al.. "Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene." Acta Dermato-Venereologica, vol. 97, no. 1, 2017, pp. 108-109.
APA	Youssefian L, Vahidnezhad H, Aghighi Y, Ziaee V, Zeinali S, Abiri M, Uitto J (2017). Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene. Acta Dermato-Venereologica, 97(1), 108-109.
Chicago	Youssefian L, Vahidnezhad H, Aghighi Y, Ziaee V, Zeinali S, Abiri M, Uitto J. "Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene." Acta Dermato-Venereologica 97, no. 1 (2017): 108-109.
Harvard	Youssefian L et al. (2017) 'Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene', Acta Dermato-Venereologica, 97(1), pp. 108-109.
Vancouver	Youssefian L, Vahidnezhad H, Aghighi Y, Ziaee V, Zeinali S, Abiri M, et al.. Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene. Acta Dermato-Venereologica. 2017;97(1):108-109.
BibTex	@article{ author = {Youssefian L and Vahidnezhad H and Aghighi Y and Ziaee V and Zeinali S and Abiri M and Uitto J}, title = {Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene}, journal = {Acta Dermato-Venereologica}, volume = {97}, number = {1}, pages = {108-109}, year = {2017} }
RIS	TY - JOUR AU - Youssefian L AU - Vahidnezhad H AU - Aghighi Y AU - Ziaee V AU - Zeinali S AU - Abiri M AU - Uitto J TI - Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the Cmg2/Antxr2 Gene JO - Acta Dermato-Venereologica VL - 97 IS - 1 SP - 108 EP - 109 PY - 2017 ER -

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