Content » Vol 97, Issue 1

Short communication

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

Leila Youssefian, Hassan Vahidnezhad, Yahya Aghighi, Vahid Ziaee, Sirous Zeinali, Maryam Abiri, Jouni Uitto
DOI: 10.2340/00015555-2459

Abstract

Abstract is missing (Short communication)

Significance

Supplementary content

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