Published in
Wiley Open Access, Molecular Genetics and Genomic Medicine, 2(9), 2020
DOI: 10.1002/mgg3.1556
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A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia
Journal article published in 2020 by
Qizong Lao 
,
Ashwini Mallappa ,
Fabio Rueda Faucz ,
Elizabeth Joyal,
Padmasree Veeraraghavan,
Wuyan Chen,
Deborah P. Merke
,
Ashwini Mallappa ,
Fabio Rueda Faucz ,
Elizabeth Joyal,
Padmasree Veeraraghavan,
Wuyan Chen,
Deborah P. Merke
This paper is made freely available by the publisher.
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