Hematologically important mutations: X-linked chronic granulomatous disease (Second update)

[1] Genetic analysis of 13 families with X-linked chronic granulomatous disease reveals a low proportion of sporadic patients and a high proportion of sporadic carriers [J]. PEDIATRIC RESEARCH, 1998, 44 (01) : 85 - 92

[2] A 15-BASE PAIR (BP) PALINDROMIC INSERTION ASSOCIATED WITH A 3-BP DELETION IN EXON-10 OF THE GP91-PHOX GENE, DETECTED IN 2 PATIENTS WITH X-LINKED CHRONIC GRANULOMATOUS-DISEASE [J]. HUMAN GENETICS, 1995, 96 (01) : 6 - 8

[3] ARIGA T, 1994, HUM GENET, V94, P441

[4] A NEWLY RECOGNIZED POINT MUTATION IN THE CYTOCHROME-B(558) HEAVY-CHAIN GENE REPLACING ALANINE(57) BY GLUTAMIC-ACID, IN A PATIENT WITH CYTOCHROME-B POSITIVE X-LINKED CHRONIC GRANULOMATOUS-DISEASE [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1993, 152 (06) : 469 - 472

[5] Ariga Tadashi, 1994, European Journal of Haematology, V52, P99

[6] A NEW MUTATION IN EXON-12 OF THE GP91-PHOX GENE LEADING TO CYTOCHROME B-POSITIVE X-LINKED CHRONIC GRANULOMATOUS-DISEASE [J]. BLOOD, 1995, 85 (11) : 3274 - 3277

[7] BOLSCHER BGJM, 1991, BLOOD, V77, P2482

[8] MOLECULAR ANALYSIS IN 3 CASES OF X91(-) VARIANT CHRONIC GRANULOMATOUS-DISEASE [J]. BLOOD, 1995, 86 (09) : 3575 - 3582

[9] CROSS AR, 1995, J BIOL CHEM, V270, P17056

[10] Hematologically important mutations: The autosomal recessive forms of chronic granulomatous disease (First update) [J]. BLOOD CELLS MOLECULES AND DISEASES, 2000, 26 (05) : 561 - +

[1] Genetic analysis of 13 families with X-linked chronic granulomatous disease reveals a low proportion of sporadic patients and a high proportion of sporadic carriers [J]. PEDIATRIC RESEARCH, 1998, 44 (01) : 85 - 92

[2] A 15-BASE PAIR (BP) PALINDROMIC INSERTION ASSOCIATED WITH A 3-BP DELETION IN EXON-10 OF THE GP91-PHOX GENE, DETECTED IN 2 PATIENTS WITH X-LINKED CHRONIC GRANULOMATOUS-DISEASE [J]. HUMAN GENETICS, 1995, 96 (01) : 6 - 8

[3] ARIGA T, 1994, HUM GENET, V94, P441

[4] A NEWLY RECOGNIZED POINT MUTATION IN THE CYTOCHROME-B(558) HEAVY-CHAIN GENE REPLACING ALANINE(57) BY GLUTAMIC-ACID, IN A PATIENT WITH CYTOCHROME-B POSITIVE X-LINKED CHRONIC GRANULOMATOUS-DISEASE [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1993, 152 (06) : 469 - 472

[5] Ariga Tadashi, 1994, European Journal of Haematology, V52, P99

[6] A NEW MUTATION IN EXON-12 OF THE GP91-PHOX GENE LEADING TO CYTOCHROME B-POSITIVE X-LINKED CHRONIC GRANULOMATOUS-DISEASE [J]. BLOOD, 1995, 85 (11) : 3274 - 3277

[7] BOLSCHER BGJM, 1991, BLOOD, V77, P2482

[8] MOLECULAR ANALYSIS IN 3 CASES OF X91(-) VARIANT CHRONIC GRANULOMATOUS-DISEASE [J]. BLOOD, 1995, 86 (09) : 3575 - 3582

[9] CROSS AR, 1995, J BIOL CHEM, V270, P17056

[10] Hematologically important mutations: The autosomal recessive forms of chronic granulomatous disease (First update) [J]. BLOOD CELLS MOLECULES AND DISEASES, 2000, 26 (05) : 561 - +