ADAMTSL2 autosomal dominant


Steinle  J et al. ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disorders. Am J Med Genet A. 2021;185(3):743-752. PMID: 33369194.

Desai A et al. Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos syndrome variant. BMC Musculoskelet Disord. 2016;17:80. PMID: 26879370.