Common mutation underlying primary hyperoxaluria type1 in three Indian children.
about
Primary hyperoxaluria in populations of Pakistan origin: results from a literature review and two major registries.Primary Hyperoxaluria Type 1 with Homozygosity for a Double-mutated AGXT Allele in a 2-year-old Child.Clinical and Genetic Profile of Indian Children with Primary Hyperoxaluria.Recurrent truncating mutations in alanine-glyoxylate aminotransferase gene in two South Indian families with primary hyperoxaluria type 1 causing later onset end-stage kidney disease
P2860
Common mutation underlying primary hyperoxaluria type1 in three Indian children.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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name
Common mutation underlying primary hyperoxaluria type1 in three Indian children.
@en
Common mutation underlying primary hyperoxaluria type1 in three Indian children.
@nl
type
label
Common mutation underlying primary hyperoxaluria type1 in three Indian children.
@en
Common mutation underlying primary hyperoxaluria type1 in three Indian children.
@nl
prefLabel
Common mutation underlying primary hyperoxaluria type1 in three Indian children.
@en
Common mutation underlying primary hyperoxaluria type1 in three Indian children.
@nl
P2093
P2860
P356
P1476
Common mutation underlying primary hyperoxaluria type1 in three Indian children
@en
P2093
P2860
P304
P356
10.4103/0971-4065.106044
P577
2012-11-01T00:00:00Z