Developmental and degenerative features in a complicated spastic paraplegia

Annals of Neurology

Volumn 67, Issue 4, 2010, Pages 516-525

  Manzini, M Chiara ^a   Rajab, Anna ^b   Maynard, Thomas M ^c   Mochida, Ganeshwaran H ^a,d,e   Tan, Wen Hann ^e   Nasir, Ramzi ^e   Sean Hill, R ^a   Gleason, Danielle ^e   Saffar, Muna Al ^a,e   Partlow, Jennifer N ^a,e   Barry, Brenda J ^a,e   Vernon, Mike ^c   LaMantia, Anthony Samuel ^c   Walsh, Christopher A ^a,e  

^a HARVARD MEDICAL SCHOOL   (United States)

^b MINISTRY OF HEALTH   (Oman)

^c UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^d MASSACHUSETTS GENERAL HOSPITAL   (United States)

^e BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; GENOMIC DNA; MESSENGER RNA;

ADOLESCENT; ADULT; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; CHILD; CLINICAL ARTICLE; COGNITIVE DEFECT; EMBRYO; EMBRYO DEVELOPMENT; FAMILY STUDY; FEMALE; GENE; GENE DELETION; GENE EXPRESSION; GENE MUTATION; GENETIC LINKAGE; HUMAN; HUMAN CELL; HUMAN TISSUE; IN SITU HYBRIDIZATION; LIMB DEVELOPMENT; MALE; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PARAPLEGIA; PEDIGREE ANALYSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SPASTIC PARESIS; SPG20 GENE; SYNDROME; SYNDROME DELINEATION; TROYER SYNDROME;

ADOLESCENT; ADULT; CHILD, PRESCHOOL; CHROMOSOME MAPPING; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; NEURODEGENERATIVE DISEASES; OMAN; PARAPLEGIA; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; RNA, MESSENGER; YOUNG ADULT;

EID: 77951740940     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.21923     Document Type: Article

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