C3229 PDF DOWNLOAD

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C3229 Pdf Download

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Orphanet J Rare Dis. Authors and Affiliations.

South Med J. Linkage of Marfan syndrome and aphenotypically related disorder to two different fibrillin genes.

All of these mutations reduce the amount of fibrillin-2 available to form microfibrils. The clinical symptoms are similar, but genetically distinct, to MFS. CS and XL co-authored the draft of co-manuscript.

J Bone Joint Surg Am. Apropos of a case in a newborn infant.

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