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

✍ Scribed by Laura E. Warner; Benjamin B. Roa; James R. Lupski

• Publisher: John Wiley and Sons
• Year: 1996
• Tongue: English
• Weight: 312 KB
• Volume: 8
• Category: Article
• ISSN: 1059-7794
• DOI: 10.1002/(sici)1098-1004(1996)8:4<362::aid-humu10>3.0.co;2-0