Literature DB >> 27541381

Joint laxity in homozygotes for severe POU1F1 mutations.

Hanan E Shamseldin1, Sateesh Maddirevula1, Amira Nabil2, Saeed Al-Fadhil3, Saeed Al Tala3, Fowzan S Alkuraya1,4.   

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Year:  2016        PMID： 27541381     DOI： 10.1002/ajmg.a.37941

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  1 in total

1.  POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literature.

Authors:  Swati Jadhav; Chakra Diwaker; Anurag R Lila; Jugal V Gada; Shantanu Kale; Vijaya Sarathi; Puja M Thadani; Sneha Arya; Virendra A Patil; Nalini S Shah; Tushar R Bandgar
Journal:  Pituitary       Date:  2021-03-20       Impact factor: 4.107
  1 in total

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