TY  - GEN
AU  - Schwartz,Charles E
AU  - May,Melanie M
AU  - Carpenter,Nancy J
AU  - Rogers,R Curtis
AU  - Martin,Judith
AU  - Bialer,Martin G
AU  - Ward,Jewell
AU  - Sanabria,Javier
AU  - Marsa,Silvana
AU  - Lewis,James A
AU  - Echeverri,Roberto
AU  - Lubs,Herbert A
AU  - Voeller,Kytja
AU  - Simensen,Richard J
AU  - Stevenson,Roger E
TI  - Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene
SN  - 0002-9297
PY  - 2005///0829
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Child
KW  - Child, Preschool
KW  - Chromosomes, Human, X
KW  - Developmental Disabilities
KW  - genetics
KW  - Female
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - X-Linked Intellectual Disability
KW  - Middle Aged
KW  - Monocarboxylic Acid Transporters
KW  - Muscle Weakness
KW  - Mutation
KW  - Paraplegia
KW  - Pedigree
KW  - Symporters
N1  - Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1086/431313
ER  -