Novel compound heterozygous laminina2-chain gene (LAMA2) mutations in congenital muscular dystrophy. Mutations in brief no. 159. Online.

Human mutation

Volumn 12, Issue 2, 1998, Pages 135-

  Mendell, J T ^a   Panicker, S G ^a   Tsao, C Y ^a   Feng, B ^a   Sahenk, Z ^a   Marzluf, G A ^a   Mendell, J R ^a  

^a OHIO STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; LAMININ; LAMININ ALPHA2;

ARTICLE; GENETICS; HETEROZYGOTE DETECTION; HUMAN; MUSCULAR DYSTROPHY; MUTATION; NUCLEOTIDE SEQUENCE;

DNA MUTATIONAL ANALYSIS; DNA, COMPLEMENTARY; HETEROZYGOTE DETECTION; HUMANS; LAMININ; MUSCULAR DYSTROPHIES; MUTATION;

MLCS; MLOWN;

EID: 0032222725     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1098-1004(1998)12:2<135::aid-humu10>3.3.co;2-y     Document Type: Article

References (0)