Erratum: finckh U, Schroder J, ressler B, veske A, gal A. Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease. Am J med genet 92:40-46
Am J Med Genet
.
2000 Oct 23;94(5):438.
Authors
M Ghadami
1
,
HA Tomita
,
MT Najafi
,
E Damavandi
,
MS Farahvash
,
K Yamada
,
K Majidzadeh-A
,
N Niikawa
Affiliation
1
Department of Human Genetics, Nagasaki University School of Medicine, Nagasaki, Japan.
PMID:
11050633
No abstract available