Gene: [11p155/AMCD2B] arthrogryposis multiplex congenita, distal, type 2B; Freeman-Sheldon syndrome variant; [DA2B ]

REL

GEM:09^/IBM2; GEM:0X^/AMCD.

REF

REV,PAT,NOM "Bamshad M &: Am J Med Genet, 65, N4, 277-281, 1996
LIN,LOC "Bamshad M &: AJHG, 55, 1153-1158, 1994
PAT "Klemp P, Hall JG: Am J Med Genet, 55, N4, 414-419, 1995
PAT "Krakowiak PA &: Am J Med Genet, 76, N1, 93-98, 1998
LIN,LOC "Krakowiak PA &: AJHG, 60, N2, 426-432, 1997

KEY

myo, devd

CLA

unknown, basic

LOC

11 p15.5

MIM

MIM: 601680

SYN

DA2B

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