Giant axonal neuropathy locus refinement to a < 590 kb critical interval.

Cavalier, L; BenHamida, C; Amouri, R; Belal, S; Bomont, P; Lagarde, N; Gressin, L; Callen, D; Demir, E; Topaloglu, H; Landrieu, P; Ioos, C; Hamida, M B; Koenig, M; Hentati, F

Cavalier, L; BenHamida, C; Amouri, R; Belal, S; Bomont, P; Lagarde, N; Gressin, L; Callen, D; Demir, E; Topaloglu, H; Landrieu, P; Ioos, C; Hamida, M B; Koenig, M; Hentati, F.

Affiliation

Cavalier L; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, CU de Strasbourg, France.

Eur J Hum Genet ; 8(7): 527-34, 2000 Jul.

Article in En | MEDLINE | ID: mdl-10909853

Subject(s)

Axons/pathology; Bone and Bones/abnormalities; Contig Mapping; Intellectual Disability/genetics; Menkes Kinky Hair Syndrome/genetics; Neurodegenerative Diseases/genetics; Chromosome Mapping; Chromosomes, Human, Pair 16/genetics; Consanguinity; DNA Primers/chemistry; Female; Haplotypes; Homozygote; Humans; Intellectual Disability/pathology; Linkage Disequilibrium; Male; Menkes Kinky Hair Syndrome/pathology; Microsatellite Repeats; Neurodegenerative Diseases/pathology; Pedigree; Physical Chromosome Mapping; Polymerase Chain Reaction; Polymorphism, Genetic; Polyneuropathies/genetics; Polyneuropathies/pathology

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Database: MEDLINE Main subject: Axons / Bone and Bones / Neurodegenerative Diseases / Contig Mapping / Menkes Kinky Hair Syndrome / Intellectual Disability Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Year: 2000 Type: Article

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