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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