Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTC
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Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTC. / Jakubiczka, Sibylle; Bettecken, Thomas; Mohnike, Klaus; Schneppenheim, Reinhard; Stumm, Markus; Tönnies, Holger; Volleth, Marianne; Wieacker, Peter.
In: EUR J PEDIATR, Vol. 166, No. 7, 07.2007, p. 743-5.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTC
AU - Jakubiczka, Sibylle
AU - Bettecken, Thomas
AU - Mohnike, Klaus
AU - Schneppenheim, Reinhard
AU - Stumm, Markus
AU - Tönnies, Holger
AU - Volleth, Marianne
AU - Wieacker, Peter
PY - 2007/7
Y1 - 2007/7
N2 - A contiguous deletion encompassing the genes for dystrophin, cytochrome b(-245) beta-subunit (CYBB), retinitis pigmentosa GTPase regulator (RPGR), and OTC was detected in a female patient only suffering from OTC deficiency while symptoms of the other conditions were not present.
AB - A contiguous deletion encompassing the genes for dystrophin, cytochrome b(-245) beta-subunit (CYBB), retinitis pigmentosa GTPase regulator (RPGR), and OTC was detected in a female patient only suffering from OTC deficiency while symptoms of the other conditions were not present.
KW - Child, Preschool
KW - Chromosomes, Human, X
KW - Dystrophin
KW - Eye Proteins
KW - Female
KW - Gene Deletion
KW - Heterozygote
KW - Humans
KW - Membrane Glycoproteins
KW - NADPH Oxidase
KW - Ornithine Carbamoyltransferase Deficiency Disease
KW - Pedigree
U2 - 10.1007/s00431-006-0303-0
DO - 10.1007/s00431-006-0303-0
M3 - SCORING: Journal article
C2 - 17091258
VL - 166
SP - 743
EP - 745
JO - EUR J PEDIATR
JF - EUR J PEDIATR
SN - 0340-6199
IS - 7
ER -