Min Wang

Fatal perinatal mitochondrial cardiac failure caused by recurrent de novo duplications in the ATAD3 locus.

Jafar S. Jabbari, V. Mootha, Y. Okazaki, 2020, Med.

Clinicopathological and genetic analysis of Aicardi-Goutières syndrome

Min Wang, Hongwei Guo, N. Mao, 2014 .

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

S. Züchner, M. Lek, F. Muntoni, 2013, Brain : a journal of neurology.

Epidermoid cyst in a patient with Alagille syndrome: Coincidence or connection?

J. Kuo, Min Wang, R. Ashour, 2020, Surgical neurology international.

[Pathology and molecular pathogenesis of spondyloepiphyseal dysplasia tarda with progressive arthropathy caused by compound CCN6 heterogeneous gene mutations].

Ling-Qing Yuan, Xiang-hang Luo, E. Liao, 2004, Zhonghua yi xue za zhi.

Thyroid hormone resistance syndrome caused by heterozygous A317T mutation in thyroid hormone receptor β gene

Min Wang, Ju-ming Lu, Q. Guo, 2016, Medicine.

Thyroid hormone resistance syndrome caused by heterozygous A317T mutation in thyroid hormone receptor β gene

Min Wang, Ju-ming Lu, Q. Guo, 2016, Medicine.