... 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 ...

... disorder, named types A, B, and C (or complementation groups A, B, and C). The forms have the same signs and symptoms but are distinguished by their genetic cause: MOCS1 gene mutations cause type A, MOCS2 gene mutations cause type ...

... Genetic Testing Registry: Bare lymphocyte syndrome, type II, complementation group c ... A, Reith W, Puck JM, Cheng LE. Novel Mutation in the Class II Transactivator Associated with Immunodeficiency ...

... available. Citation on PubMed Bontron S, Steimle V, Ucla C, Eibl ... and Its Dual Roles in MHC Gene Transcription. Front Immunol. 2013 Dec 20;4:476. ...

... published></gene-summary><gene-summary ><gene-symbol >FANCC</gene-symbol><name >FA complementation group C</name><ghr-page >https://medlineplus.gov/genetics/gene/ ...

... form of the disorder designated type B or complementation group B. The MOCS2 gene mutations involved in molybdenum cofactor deficiency likely eliminate the ...

... gene/fanca</url></topic><topic ><title >FANCC: FA complementation group C</title><url >https://medlineplus.gov/genetics/gene/fancc</url></topic><topic ><title >FANCG: FA complementation ...

... About This Health Condition Other Names for This Gene FAC FACC FANCC_HUMAN Fanconi anemia complementation group C Fanconi anemia, complementation group C Additional Information & Resources ...