TY  - GEN
AU  - Abdel-Hamid,M S
AU  - Issa,M Y
AU  - Otaify,G A
AU  - Abdel-Ghafar,S F
AU  - Elbendary,H M
AU  - Zaki,M S
TI  - PGAP3-related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation
SN  - 1399-0004
PY  - 2018///0806
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Base Sequence
KW  - Carboxylic Ester Hydrolases
KW  - Consanguinity
KW  - Egypt
KW  - Family Health
KW  - Female
KW  - Founder Effect
KW  - Genetic Predisposition to Disease
KW  - Homozygote
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Phenotype
KW  - Phosphorus Metabolism Disorders
KW  - Receptors, Cell Surface
KW  - Sequence Analysis, DNA
KW  - methods
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1111/cge.13033
ER  -