SCOPUS 정보 검색 플랫폼

Volumn 107, Issue 3, 2002, Pages 256-258

Exclusion of mutations in the MTMR1 gene as a frequent cause of X-linked myotubular myopathy [4]

(8) Herman, Gail E a Kopacz, Kevin a Zhao, Wei D a Copley, LaRae M a Poustka, Annemarie b Kioschis, Petra b Platzer, Matthias c Taudien, Stefan c

a OHIO STATE UNIVERSITY (United States)

b GERMAN CANCER RESEARCH CENTER DKFZ (Germany)

c FRITZ LIPMANN INSTITUTE (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CENTRONUCLEAR MYOPATHY; CHROMOSOMAL LOCALIZATION; GENE FREQUENCY; GENE MUTATION; HUMAN; LETTER; MUSCLE BIOPSY; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

DNA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; HUMANS; LINKAGE (GENETICS); MALE; MUTATION; MYOPATHIES, STRUCTURAL, CONGENITAL; PEDIGREE; PROTEIN-TYROSINE-PHOSPHATASE; X CHROMOSOME;

EID: 0037154063 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10135 Document Type: Letter

Times cited : (6)

References (12)

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2
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.