id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_arndyvdyobgtlpeh4rho7pywpi	M.Esther Gallardo	The Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism	2001	13	.pdf	application/pdf	7797	720	63	The 19-exon MCCA gene maps to 3q25-27 and encodes a 725-residue protein with a biotin attachment site; the 17-exon MCCB gene maps to 5q12-q13 and encodes a 563-residue polypeptide. "CGB." We detected two MCCA missense mutations in CGA patients, one of which leads to absence of biotinylated b Used both in mutation screening and/or SSCP analysis with human genomic DNA as template and in RH mapping. A lEMBL4 library was screened with fungal EST candidates (Fungal Genetics Stock Center) for genes encoding MCCa or MCCb. The cloned inserts in two partially Figure 1 cDNA nucleotide sequence and intron-exon organization of human MCCA and MCCB. the cDNA level, the human MCCA and MCCB genes MCG; and we have detected six MCCA or MCCB mutations in patients diagnosed with the disease. Mutations in MCCA or MCCB, in Patients with MCG Mutations in MCCA or MCCB, in Patients with MCG Mutations in MCCA or MCCB, in Patients with MCG	./cache/work_arndyvdyobgtlpeh4rho7pywpi.pdf	./txt/work_arndyvdyobgtlpeh4rho7pywpi.txt