Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Dante M. LaMorticella"'
Publikováno v:
Cytogenetics and cell genetics. 86(1)
Small-conductance, calcium-activated potassium channels contribute to the afterhyperpolarization in central neurons and other cell types. Because these channels regulate neuronal excitability, defects in their genes could cause excitability disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e282114a417c652f686c9d57ded9a1
https://pubmed.ncbi.nlm.nih.gov/10516439
https://pubmed.ncbi.nlm.nih.gov/10516439
Autor:
Dante M. LaMorticella, William H. Murphey, Patricia L. Kramer, Michael Litt, Everett W. Lovrien, Richard G. Weleber
Publikováno v:
Human molecular genetics. 7(3)
Congenital cataracts are a common major abnormality of the eye that frequently cause blindness in infants. At least a third of all cases are familial; autosomal dominant congenital cataract (ADCC) appears to be the most common familial form in the We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e02617e98af320dfe4b57365b01dbe1b
https://pubmed.ncbi.nlm.nih.gov/9467006
https://pubmed.ncbi.nlm.nih.gov/9467006
Autor:
Dennis W. Schultz, Dante M. LaMorticella, Roque D. Carrero-Valenzuela, Michael Litt, Irene H. Maumenee, Thomas N. Mitchell, Patricia L. Kramer
Publikováno v:
Human molecular genetics. 6(5)
Congenital cataracts are a common major abnormality of the eye that frequently cause blindness in infants. At least a third of all cases are familial; autosomal dominant congenital cataract (ADCC) appears to be the most common familial form in the We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ede772f7cc74e6aa538155de03c2211
https://pubmed.ncbi.nlm.nih.gov/9158139
https://pubmed.ncbi.nlm.nih.gov/9158139
Autor:
Dante M. LaMorticella, Patricia L. Kramer, Roque D. Carrero-Valenzuela, Everett W. Lovrien, Irene H. Maumenee, Thomas N. Mitchell, Jennifer Yount, Michael Litt
Publikováno v:
Genomics. 35(3)
Congenital cataracts are one of the most common major eye abnormalities and often lead to blindness in infants. At least a third of all cases are familial. Within this group, highly penetrant, autosomal dominant forms of congenital cataracts (ADCC) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0623b02c78ddbdeb27b85803ad3e5eb8
https://pubmed.ncbi.nlm.nih.gov/8812489
https://pubmed.ncbi.nlm.nih.gov/8812489