TY  - GEN
AU  - Klaassens,M
AU  - Blom,E W
AU  - Schrander,J J P
AU  - Ris-Stalpers,C
AU  - Nieuwenhuijzen Kruseman,A C
AU  - van Steensel,M A M
AU  - Schrander-Stumpel,C T R M
TI  - Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation
SN  - 1365-2133
PY  - 2010///0920
KW  - Chromogranins
KW  - Fibrous Dysplasia, Polyostotic
KW  - genetics
KW  - GTP-Binding Protein alpha Subunits, Gs
KW  - Humans
KW  - Infant
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Pseudohypoparathyroidism
KW  - Skin
KW  - pathology
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1365-2133.2009.09543.x
ER  -