Gene: [0Xq2/IP2] incontinentia pigmenti, type II (familial; male-lethal);
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HET |
The gene for a sporadic form of incontinentia pigmenti manifesting, as a rule, in the cases X chromosome rearrangements, is mapped in X chr (GEM:0Xp11/IP1)." |
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REF |
LOC,LIN,MAP "Sefiani A &: CCG, 51, (HGM10), 1076, 1989a LOC,LIN,MAP "Sefiani A &: Genomics, 4, 427-429, 1989b LOC,LIN,MAP "Sefiani A &: Hum Genet, 80, 282-286, 1988 |
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KEY |
derm |
|
CLA |
unknown, basic |
|
LOC |
0X q27-28 |
|
MIM |
MIM: 308310 |
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