Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene. [electronic resource]
Producer: 20050829Description: 41-53 p. digitalISSN:- 0002-9297
- Adolescent
- Adult
- Aged
- Child
- Child, Preschool
- Chromosomes, Human, X
- Developmental Disabilities -- genetics
- Female
- Humans
- Infant
- Infant, Newborn
- Male
- X-Linked Intellectual Disability -- genetics
- Middle Aged
- Monocarboxylic Acid Transporters -- genetics
- Muscle Weakness -- genetics
- Mutation
- Paraplegia -- genetics
- Pedigree
- Symporters
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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.
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