Rare cases of congenital arthrogryposis multiplex caused by novel recurrent CHRNG mutations
Jieun Seo(Yokohama National University), Yong Beom Shin(Pusan National University Hospital), In-Ho Choi(Seoul National University), Je‐Sang Lee(Gachon University Gil Medical Center), Nayoung K. D. Kim(Samsung Medical Center), Murim Choi(Seoul National University), Yongjin Yoo(Korea University), Jung Min Ko(Ulsan College)
Cited by 22
Related Papers
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
|Neuron|2011|1.3k
K <sup>+</sup> Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension
|Science|2011|983