ABSENCE OF PMP22 CODING REGION MUTATIONS IN CMT1A DUPLICATION PATIENTS - FURTHER EVIDENCE SUPPORTING GENE DOSAGE AS A MECHANISM FOR CHARCOT-MARIE-TOOTH DISEASE TYPE 1A

Authors
WARNER LE ROA BB LUPSKI JR
Citation
Le. Warner et al., ABSENCE OF PMP22 CODING REGION MUTATIONS IN CMT1A DUPLICATION PATIENTS - FURTHER EVIDENCE SUPPORTING GENE DOSAGE AS A MECHANISM FOR CHARCOT-MARIE-TOOTH DISEASE TYPE 1A, Human mutation, 8(4), 1996, pp. 362-365
Citations number
24
Categorie Soggetti
Genetics & Heredity
Journal title
Human mutation → ACNP
ISSN journal
10597794
Volume
8
Issue
4
Year of publication
1996
Pages
362 - 365
Database
ISI
SICI code
1059-7794(1996)8:4<362:AOPCRM>2.0.ZU;2-8