Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The role of molecular genetics in diagnosing familial hematuria(s)

18 Jun 2011

Abstract excerpt

Familial microscopic hematuria (MH) of glomerular origin represents a heterogeneous group of monogenic conditions involving several genes, some of which remain unknown. Recent advances have increased our understanding and our ability to use molecular genetics for diagnosing such patients, enabling us to study their clinical characteristics over time. Three collagen IV genes, COL4A3, COL4A4, and COL4A5 explain the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cell Adhesion Molecules Research
Share to Coagulation, Bradykinin, Polyphosphates, and Angioedema
Share to Renal Diseases and Glomerulopathies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 21688191
DOI: 10.1007/s00467-011-1935-5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The role of molecular genetics in diagnosing familial hematuria(s)PMID 21688191Read ↗

Molecular genetics of familial hematuric diseases.Semantic proximity Read ↗

Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.Semantic proximity Read ↗

Familial hematuria: A review.Semantic proximity Read ↗

Identification of Co-Existence of Alport Syndrome and C3 Glomerulonephritis in A Proband with Family HistorySemantic proximity Read ↗

Alport syndrome and Alport kidney diseases - elucidating the disease spectrum.Semantic proximity Read ↗

Identification of co-existence of Alport syndrome and C3 glomerulonephritis in a proband with family history Semantic proximity Read ↗

COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?Semantic proximity Read ↗

Co-existence of Alport syndrome and C3 glomerulonephritis in a proband with family history.Semantic proximity Read ↗

Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group.Semantic proximity Read ↗

Population-based studies reveal an additive role of type IV collagen variants in hematuria and albuminuria.Semantic proximity Read ↗

COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family.Semantic proximity Read ↗

Heterozygous COL4A3/COL4A4 mutations: the hidden part of the iceberg?Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.