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Screening for nuclear genetic defects in the ATP synthase‐associated genes TMEM70, ATP12 and ATP5E in patients with 3‐methylglutaconic aciduria
Author(s) -
Tort F,
del Toro M,
Lissens W,
Montoya J,
FernàndezBurriel M,
Font A,
Buján N,
NavarroSastre A,
LópezGallardo E,
Arranz JA,
Riudor E,
Briones P,
Ribes A
Publication year - 2011
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2011.01650.x
Subject(s) - microbiology and biotechnology , biology , genomic dna , polymerase chain reaction , protein subunit , oligonucleotide , genetics , restriction fragment length polymorphism , gene , mitochondrial dna , exon , polymerase
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