Bone Reports
(Apr 2021)
Novel heterozygous mutations in gene SERPINH1 cause autosomal recessive osteogenesis imperfecta type X
Affiliations
- Liliana Mejia Zapata
- Corresponding author.; Fundación Clinica Valle del Lili y Clinica Infantil Club Noel, Valle de Cauca, Cali, Colombia
- Journal volume & issue
-
Vol. 14
p.
100994
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