Mutation of the Type X Collagen Gene (COL10A1) Causes Spondylometaphyseal Dysplasia

American Journal of Human Genetics - United States
doi 10.1086/302158
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Elsevier BV

Related search

Spondylometaphyseal Dysplasia, Schmidt Type

2020English

Spondylometaphyseal Dysplasia

2020English

Axial Spondylometaphyseal Dysplasia

2020English

Tissue-Specific Regulation of the Type X Collagen Gene:

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
1995English

Spondylometaphyseal Dysplasia-Cone-Rod Dystrophy Syndrome

2020English

A Recurrent 1992delCT Mutation of the Type X Collagen Gene in a Japanese Patient With Schmid Metaphyseal Chondrodysplasia

Japanese journal of human genetics
1996English

Multiple Transcriptional Elements in the Avian Type X Collagen Gene

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
1998English

Null Mutation of the Endothelin Receptor Type B Gene Causes Embryonic Death in the GK Rat

PLoS ONE
Multidisciplinary
2019English

A Missense Mutation, p.V132G, in the X-Linked Spermine Synthase Gene (SMS) Causes Snyder-Robinson Syndrome

American Journal of Medical Genetics, Part A
Genetics
2009English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy