- ... form of the disorder designated type B or complementation group B. The MOCS2 gene mutations involved in molybdenum cofactor deficiency likely eliminate the ...
- ... FANCE 602774 RAD51 PARALOG C; RAD51C 602956 FANCG GENE; FANCG 603467 FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF 604094 MITOTIC ARREST-DEFICIENT 2 LIKE 2; ...
- ... Moser HW, Suzuki Y, Kondo N, Fujiki Y. Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. Am J ...
- ... 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 ...
- ... 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 ...
- ... COMPLEMENTATION GROUP A; FANCA FANCONI ANEMIA, COMPLEMENTATION GROUP F; ... GENE; FANCM FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG FANCONI ...
- ... Disorders (NORD) Clinical Trials ClinicalTrials.gov ... GROUP F; XPF XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG XERODERMA ...
- ... syndrome. Additionally, it is unknown why the Trp361Cys mutation causes photosensitivity without the ... group 8 excision repair cross-complementing rodent repair deficiency, ...
- ... TJ, Rosenblatt DS, Gravel RA. Identification of the gene responsible for the cblB complementation group ... F, Baumgartner MR, Viardot C, Suormala T, Burgard P, ...
- ... syndrome. Additionally, it is unknown why the Arg77Ter mutation causes photosensitivity without the other ... (yeast) homolog Additional Information & Resources ...
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