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

[Responses to a reader's question on the article "Clinical and genetic analyses of a family with atypical nonketotic hyperglycinemia caused by compound heterozygous"].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 1 Jun 2021

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Genetic Testing
Share to Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 34130791
PMCID: PMC8213991

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

[Responses to a reader's question on the article "Clinical and genetic analyses of a family with atypical nonketotic hyperglycinemia caused by compound heterozygous"].PMID 34130791Read ↗

[A family with hereditary FⅪ deficiency caused by compound heterozygous mutation].Semantic proximity Read ↗

[A case of classic nonketotic hyperglycinemia caused by compound heterozygous mutation of GLDC gene].Semantic proximity Read ↗

[Nonketotic hyperglycinemia].Semantic proximity Read ↗

[Clinical and genetic analyses of a family with atypical nonketotic hyperglycinemia caused by compound heterozygous mutations in the GLDC gene].Semantic proximity Read ↗

[Diabetes caused by glucokinase mutation].Semantic proximity Read ↗

[A new mutation in the GLDC gene in non-ketotic hyperglycinaemia].Semantic proximity Read ↗

[Hemochromatosis: the importance of mutation screening in the family].Semantic proximity Read ↗

[Genetic analysis in families with histidinemía (author's transl)].Semantic proximity Read ↗

[Gene mutations in familial hyperlipidemias].Semantic proximity Read ↗

[Genetic diagnosis of pheochromocytoma].Semantic proximity Read ↗

[Gene mutations responsible for hyperlipoproteinemia].Semantic proximity Read ↗

[Compound heterocygosis for intron 9 + 1 g > T and Leu850pro mutations in the SLC12A3 gene in Gitelman's syndrome].Semantic proximity Read ↗

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