Associated Papers
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
Khan MJ et al.
Scientific Reports, 2018
30389958 (PubMed )
Supplement: 41598_2018_34262_MOESM2_ESM.xlsx › 3._co-segregation
SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures.
Wang J et al.
Bmc Medical Genetics, 2017
Genetic variations of the MCT4 (SLC16A3) gene in the Chinese and Indian populations of Singapore.
Lean CB et al.
Drug Metabolism and Pharmacokinetics, 2012
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