P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye.
about
Heritable Skeletal Disorders Arising from Defects in Processing and Transport of Type I Procollagen from the ER: Perspectives on Possible Therapeutic Approaches.Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome.Proline hydroxylation in collagen supports integrin binding by two distinct mechanisms.Impact of energy restriction during late gestation on the muscle and blood transcriptome of beef calves after preconditioning
P2860
P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye.
description
2017 nî lūn-bûn
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P4HA1 mutations cause a unique ...... don, bone, muscle and the eye.
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P4HA1 mutations cause a unique ...... don, bone, muscle and the eye.
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P4HA1 mutations cause a unique ...... don, bone, muscle and the eye.
@en
P4HA1 mutations cause a unique ...... don, bone, muscle and the eye.
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P4HA1 mutations cause a unique ...... don, bone, muscle and the eye.
@en
P4HA1 mutations cause a unique ...... don, bone, muscle and the eye.
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P2093
P2860
P50
P356
P1476
P4HA1 mutations cause a unique ...... ndon, bone, muscle and the eye
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P2093
A Reghan Foley
Antti M Salo
Carsten G Bönnemann
Elena Makareeva
Jahannaz Dastgir
Joan C Marini
Johanna Myllyharju
Matthew A Deardorff
Meganne E Leach
Monkol Lek
P2860
P304
P356
10.1093/HMG/DDX110
P577
2017-06-01T00:00:00Z