Gene: [0Xq28/FMR2] fragile X mental retardation 2 protein; fragile X mental retardation 2; fragile site Xq28, folic acid type, rare; mental retardation, X-linked 2 (non-dysmorphic); [FRAXE Ox19 ]


REF

CLO,SEQ "Chakrabarti L &: Hum Mol Genet, 5, 275-282, 1996
CLO,SEQ,GEN "Gecz J &: Genomics, 44, N2, 201-213, 1997a
EXP "Gecz J &: Hum Mol Genet, 6, N3, 435-441, 1997b
CLO,SEQ "Gecz J &: Nature Genet, 13, N1, 105-108, 1996
CLO,SEQ "Gu Y &: Nature Genet, 13, 109-113, 1996
FUN,HET "Knight SJL &: AJHG, 58, N3, 906-913, 1996
MUT "Mila M &: Hum Genet, 100, N5-6, 503-507, 1997
LIN,LOC "Mulley JC &: Am J Med Genet, 43, 383-391, 1992
LIN,LOC "Sutherland GR &: Am J Med Genet, 30, 493-508, 1988
LIN,LOC "Suthers GK &: Am J Med Genet, 30, 485-491, 1988

KEY

chr, tri, neu, devd

CLA

coding, basic

LOC

0X q28

MIM

MIM: 309548

SYN

FRAXE Ox19

Смотрите также:

  • Gene: [0Xq273/FMR1] fragile X mental retardation 1 (Martin-Bell syndrome); fragile site Xq27.3, folic acid type, rare; Martin-Bell syndrome (mental retardation/macroorchidism); [FRAXA MRXFRA ]
  • Синдром FRAXE (синдром умственной отсталости, тип E; X-сцепленное заболевание)
  • FraXE