[Two cases of congenital myotonic dystrophy type 1 caused by <i>DMPK</i> gene variants]. [PDF]
Wang XH +6 more
europepmc +1 more source
[A case of Berry syndrome associated with <i>SOX11</i>-related Coffin-Siris syndrome type 9]. [PDF]
Wang Y, Wang Z.
europepmc +1 more source
[Adeno-associated virus-mediated gene therapy for genetic epilepsy: prospects and challenges]. [PDF]
Sun B, Wang XL, Peng J.
europepmc +1 more source
[Value of gene mutation in the prognosis and treatment of multiple myeloma]. [PDF]
Cheng LL, Zhuang JL.
europepmc +1 more source
[Diagnostic Performance of Metagenomic Next-Generation Sequencing for Mucormycosis: A Retrospective Cohort Study]. [PDF]
Zhang W, Zhong S, Lu S, Xiao X, Xie Y.
europepmc +1 more source
[The cochlear extracellular matrix gene mutations and hearing loss]. [PDF]
Wang Q, Yuan Y, Han W.
europepmc +1 more source
[A case of Harel-Yoon syndrome with seizures caused by an ATAD3A variant]. [PDF]
Yang Q, Pan Z, Chen C, Yin F, Peng J.
europepmc +1 more source
[Relationship between family trauma, school bullying and suicidal behavior in adolescents: Regulatory effect of <i>DRD2</i> gene polymorphism]. [PDF]
Bai H, Chen Y, Wang K, Xu X.
europepmc +1 more source
[A case report of primary hypomagnesemia with secondary hypocalcemia caused by <i>TRPM6</i> gene variants]. [PDF]
Zhou MY, Tang XJ, Lin SX, Chen CF.
europepmc +1 more source
[Acute megakaryoblastic leukemia with CBFA2T3::GLIS2 fusion gene: 3 cases report and literature review]. [PDF]
Lin S +7 more
europepmc +1 more source

