A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36

Neurology

Volumn 67, Issue 1, 2006, Pages 120-124

  Maystadt, I ^a,e   Zarhrate, M ^a   Leclair Richard, D ^d   Estournet, B ^f   Barois, A ^f   Renault, F ^b   Routon, M C ^b   Durand, M C ^d   Lefebvre, S ^c   Munnich, A ^a   Verellen Dumoulin, C ^e   Viollet, L ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b ARMAND TROUSSEAU HOSPITAL   (France)

^c INSTITUT JACQUES MONOD   (France)

^d RAYMOND POINCARÉ HOSPITAL   (France)

^e UNIVERSITÉ CATHOLIQUE DE LOUVAIN   (Belgium)

^f NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AFRICA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 1P; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE SEVERITY; FEMALE; GENE; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; GENOMICS; HOMOZYGOSITY; HUMAN; MALE; MOTOR NEURON DISEASE; MUSCLE WEAKNESS; ONSET AGE; PRIORITY JOURNAL; SCHOOL CHILD; SMN1 GENE; SOD1 GENE; CHILD; CHROMOSOME 1; CHROMOSOME MAP; COMPARATIVE STUDY; GENETICS; METHODOLOGY; RECESSIVE GENE;

ADOLESCENT; ADULT; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; GENES, RECESSIVE; HUMANS; LINKAGE (GENETICS); MALE; MOTOR NEURON DISEASE;

EID: 33746801641     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000223834.55225.2d     Document Type: Article

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