Associated Papers
Rickets manifestations in a child with metaphyseal anadysplasia, report of a spontaneously resolving case.
Diaz Escagedo P et al.
Bmc Pediatrics, 2021
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage.
Komor AC et al.
Nature, 2016
27096365 (PubMed )
Supplement: NIHMS774092-supplement-1.pdf
MMP13 mutations are the cause of recessive metaphyseal dysplasia, Spahr type.
Bonafé L et al.
American Journal of Medical Genetics. Part A, 2014
Metaphyseal anadysplasia type 1: Familial and regressive rickets manifestation.
Matsumoto H et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 0
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