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Molybdenum cofactor "deficiency," complementation group B
Did you mean Molybdenum factors "deficiency," implementation group B?
- ... gov MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC ...
- ... form of the disorder designated type B or complementation group B.The MOCS2 gene mutations involved in molybdenum cofactor deficiency likely eliminate the function of MOCS2A, MOCS2B, or ...
- ... form of the disorder designated type C or complementation group C. This is the rarest form of the condition, affecting only a small number of individuals.The GPHN gene mutations involved in molybdenum cofactor deficiency likely reduce or eliminate the function of gephyrin. ...
- ... form of the disorder designated type A or complementation group A. This is the most common form of the condition, accounting for approximately two-thirds of cases.The MOCS1 gene mutations involved in molybdenum cofactor deficiency likely eliminate the function of MOCS1A, MOCS1B, or ...