A whole-genome scan in a large family with leukodystrophy and oligodontia reveals linkage to 10q22

Neurogenetics

Volumn 12, Issue 1, 2011, Pages 73-78

  Chouery, Eliane ^a   Delague, Valérie ^b   Jalkh, Nadine ^a   Salem, Nabiha ^a   Kfoury, Jessy ^a   Rodriguez, Diana ^c,i   Chabrol, Brigitte ^d   Boespflug Tanguy, Odile ^e   Lévy, Nicolas ^b   Serre, Jean Louis ^f   Mégarbané, André ^a,g,h  

^a SAINT JOSEPH UNIVERSITY   (Lebanon)

^b AIX MARSEILLE UNIVERSITY   (France)

^c ARMAND TROUSSEAU HOSPITAL   (France)

^d TIMONE HOSPITAL   (France)

^e HÔPITAL ROBERT DEBRÉ   (France)

^f LABORATOIRE DES SCIENCES DU CLIMAT ET DE L ENVIRONNEMENT   (France)

^g Institut Jerome Lejeune   (France)

^h Saint Joseph University   (France)

ⁱ SORBONNE UNIVERSITÉ   (France)

Author keywords

Leukodystrophy; Linkage analysis; Microsatellite markers; Oligodontia; SNP markers

Indexed keywords

PROSAPOSIN;

ADOLESCENT; ADULT; ARTICLE; ATAXIA; BRAIN CORTEX ATROPHY; CHILD; CHROMOSOME 10Q; CLINICAL ARTICLE; DISEASE ASSOCIATION; FEMALE; GENE IDENTIFICATION; GENE LOCUS; GENE SEQUENCE; GENETIC ASSOCIATION; GENOME ANALYSIS; HUMAN; LEUKODYSTROPHY; MALE; MICROSATELLITE MARKER; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; OLIGODONTIA; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PYRAMIDAL SIGN; RARE DISEASE; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SYRIAN ARAB REPUBLIC; WHITE MATTER;

EID: 79951542330     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-010-0256-3     Document Type: Article

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