Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31.

Familial dysautonomia (FD) is an autosomal recessive disorder characterized by developmental arrest in the sensory and autonomic nervous systems and by Ashkenazi Jewish ancestry. We previously had mapped the defective gene (DYS) to an 11-cM segment of chromosome 9q31-33, flanked by D9S53 and D9S105....

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Detalhes bibliográficos
Main Authors: Blumenfeld, A, Slaugenhaupt, S A, Liebert, C B, Temper, V, Maayan, C, Gill, S, Lucente, D E, Idelson, M, MacCormack, K, Monahan, M A, Mull, J, Leyne, M, Mendillo, M, Schiripo, T, Mishori, E, Breakefield, X, Axelrod, F B, Gusella, J F
Formato: Artigo
Idioma:Inglês
Publicado em: 1999
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377835/
https://ncbi.nlm.nih.gov/pubmed/10090896
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