Eric Haan
0000-0002-7310-5124
3 papers found
Refreshing results…
Marfan syndrome resulting from a rare pathogenic FBN1 variant, ascertained through a proband with IgG4 ‐related arteriopathy
Non-coding VMA21 deletions cause X-linked Myopathy with Excessive Autophagy
Lamin A/C Mutation: An Easily Missed Opportunity
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