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Connection

LINYAN MENG to Hereditary Central Nervous System Demyelinating Diseases

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This is a "connection" page, showing publications LINYAN MENG has written about Hereditary Central Nervous System Demyelinating Diseases.
LINYAN MENG
Connection Strength
0.559
Hereditary Central Nervous System Demyelinating Diseases
  1. Homozygous variants in pyrroline-5-carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophy. Am J Med Genet A. 2017 Feb; 173(2):460-470.
    View in: PubMed
    Score: 0.559
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.