透明纤维瘤病综合征：CMG2/ANTXR2基因中的一种新型突变和复发性始祖突变 - Suppr

Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene.

作者信息

Youssefian Leila, Vahidnezhad Hassan, Aghighi Yahya, Ziaee Vahid, Zeinali Sirous, Abiri Maryam, Uitto Jouni

机构信息

Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, 233 S. 10th Street, Suite 450 BLSB, Philadelphia, PA 19107, Pennsylvania, USA.

出版信息

Acta Derm Venereol. 2017 Jan 4;97(1):108-109. doi: 10.2340/00015555-2459.

DOI:10.2340/00015555-2459

PMID:27174544

Abstract

摘要

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Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene.

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