Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by José A. Caparrós-Martín
Identification of a Mutation Causing Deficient BMP1/mTLD Proteolytic Activity in Autosomal Recessive Osteogenesis Imperfecta
Human Mutation
Genetics
Related publications
Autosomal Recessive Osteogenesis Imperfecta: A Puzzle for Bone Formation, Structure and Function
Current Genetic Medicine Reports
Mutation in Kallikrein 4 Causes Autosomal Recessive Hypomaturation Amelogenesis Imperfecta
Journal of Medical Genetics
Genetics
Osteogenesis Imperfecta
Osteogenesis Imperfecta
American Journal of Obstetrics and Gynecology
Gynecology
Obstetrics
Autosomal Dominant Amelogenesis Imperfecta Associated withENAMframeshift Mutation p.Asn36Ilefs56
Clinical Genetics
Genetics
Osteogenesis Imperfecta
Osteogenesis Imperfecta
Insight to FBXO31 Novel Mutation p.Cys283Asn Causing Non‑Syndromic Autosomal Recessive Intellectual Disability Using Computational Methods
Clinical Proteomics and Bioinformatics
Osteogenesis Imperfecta
Proceedings of the Royal Society of Medicine