Related Articles
A <em>de novo</em> mutation of <em>SALL4</em> in a Chinese family with Okihiro syndrome
Wiedemann‑Steiner syndrome in a 2‑year‑old patient due to a rare nonsense <em>KMT2A</em> mutation of <em>de</em> <em>novo</em> origin: A case report
A novel de novo variant of LAMA2 contributes to merosin deficient congenital muscular dystrophy type 1A: Case report
Genetic analysis of a child with<em> SATB2</em>‑associated syndrome and literature study
Molecular diagnosis of McArdle disease using whole-exome sequencing